About Gene List Toggle Layout

PF3D7_0505500 (MSH6)

Pf3D7_05_v3:238,878..243,954(-)

Miles Classification: Core

Function and Localization

Product Description: DNA mismatch repair protein MSH6, putative

SignalP Peptide: N/A

# Transmembrane Domains: 0

EC Numbers: N/A

Curated GO (PlasmoDB):

Component GO:0032301 MutSalpha complex
Component GO:0032300 mismatch repair complex
Component GO:0005634 nucleus
Function GO:0008094 ATP-dependent activity, acting on DNA
Function GO:0003684 damaged DNA binding
Function GO:0000400 four-way junction DNA binding
Function GO:0030983 mismatched DNA binding
Process GO:0006281 DNA repair
Process GO:0036297 interstrand cross-link repair
Process GO:0043570 maintenance of DNA repeat elements
Process GO:0000710 meiotic mismatch repair
Process GO:0006298 mismatch repair
Process GO:0045910 negative regulation of DNA recombination
Process GO:0006290 pyrimidine dimer repair

Expression by stage, third quartile (Malaria Cell Atlas): No data

More info:

Resistome Mutations

Old (Pf3D7v3) Gene ID: PF3D7_0505500

Resistome Missense Mutations: P462R

Resistome Compounds with Missense Mutations: AN13762

Resistome # Samples with Disruptive Mutations: 1 (1 missense, 1 "interesting" missense)

Essentiality

Zhang Phenotype: Non - Mutable in CDS

MIS: 0.696 | MFS: -2.407 | #Insertions: 0

PlasmoGEM Phenotype: Essential (Pb ortholog: PBANKA_1105100)

  • Relative Growth Rate: 0.11 ± 0.16
  • Confidence: 5.11

RMgmDB ABS Phenotype: N/A

More info: PhenoPlasm Link

Binding Evidence

AlphaFill Uniprot ID: Q8I447

"Best" AlphaFill ligand hit: 3JD (niraparib, Local RMSD=0.11) with 7KK5 (Global RMSD=17.37)

No associated EC numbers

No evidence of orthology to BindingDB entries

Orthology Information

Ortholog Group (OrthoMCL): OG6_100652

Most Similar Human Ortholog: A0A494C0M1

TM-align score: 0.70 | RMSD: 4.5

Seq Identity: 0.3 | Length: 979 / 1350

All Human Orthologs (OrthoMCL):

ENSG00000116062 mutS homolog 6

Genetic Variation

MalariaGEN Pf7 (worldwide samples) # unique SNV/indels:

Homozygous genotype calls only

variant type common rare doubleton singleton
synonymous 12 74 48 76
disruptive 21 69 53 100
missense 16 61 48 82

Any inclusion in genotype call

variant type common rare doubleton singleton
synonymous 19 151 53 94
disruptive 42 160 89 198
missense 32 121 74 135

PlasmoDB Total SNPs: 157

Non-coding: 102 | Synonymous: 31 | Nonsynonymous: 23 | Stop Codon: 1

Protein Information

Protein length: 1350 | Molecular Weight (kDa): 156.44

UniProt ID(s): Q8I447

PDB ID(s): None

Isoelectric Point: 6.35

Protein Domain Annotations:

InterPro IPR000432 DNA mismatch repair protein MutS, C-terminal
InterPro IPR007695 DNA mismatch repair protein MutS-like, N-terminal
InterPro IPR007696 DNA mismatch repair protein MutS, core
InterPro IPR007861 DNA mismatch repair protein MutS, clamp
InterPro IPR016151 DNA mismatch repair protein MutS, N-terminal
InterPro IPR017261 DNA mismatch repair protein MutS/MSH
InterPro IPR027417 P-loop containing nucleoside triphosphate hydrolase
InterPro IPR036187 DNA mismatch repair protein MutS, core domain superfamily
InterPro IPR036678 MutS, connector domain superfamily
PFam PF00488 DNA mismatch repair protein MutS, C-terminal
PFam PF01624 DNA mismatch repair protein MutS-like, N-terminal
PFam PF05190 DNA mismatch repair protein MutS, clamp
PFam PF05192 DNA mismatch repair protein MutS, core
Superfamily SSF48334 DNA mismatch repair protein MutS, core domain superfamily
Superfamily SSF52540 P-loop containing nucleoside triphosphate hydrolase
Superfamily SSF53150 MutS, connector domain superfamily
Superfamily SSF55271 DNA mismatch repair protein MutS, N-terminal

Associated Publications

PMID Title Authors DOI
12368867 Sequence of Plasmodium falciparum chromosomes 1, 3-9 and 13. Hall N, Pain A, ..., Barrell BG 10.1038/nature01095
23181666 Organellar proteomics reveals hundreds of novel nuclear proteins in the malariaparasite Plasmodium falciparum. Oehring SC, Woodcroft BJ, ..., Voss TS 10.1186/gb-2012-13-11-r108
38390329 Mismatch repair gene MSH6 correlates with the prognosis, immune status and immunecheckpoint inhibitors response of endometrial cancer Zhou LZ, Xiao HQ, Chen J 10.3389/fimmu.2024.1302797
38394410 Clinicopathological features and evaluation of microsatellite stability ofcolorectal carcinoma with cribriform comedo pattern Gunler T, Karabagli P, ..., Korez MK 10.4103/ijpm.ijpm_194_23
38350001 Differential responses to immune checkpoint inhibitors are governed by diversemismatch repair gene alterations Khushman MM, Toboni MD, ..., Powell MA 10.1158/1078-0432.CCR-23-3004
38378964 Predicting Mismatch Repair Deficiency Status in Endometrial Cancer throughMulti-Resolution Ensemble Learning in Digital Pathology Whangbo J, Lee YS, ..., Kim KG 10.1007/s10278-024-00997-z
38404296 Gastric and duodenal cancer in individuals with Lynch syndrome: a nationwidecohort study Caspers IA, Eikenboom EL, ..., van Leerdam ME 10.1016/j.eclinm.2024.102494
38310280 Oligogenic basis of premature ovarian insufficiency: an observational study Long P, Wang L, ..., Xiao H 10.1186/s13048-024-01351-1
38297508 Benign Adenomyoepithelioma: An Unrecognised Precursor of Ductal Carcinoma in Situin Patient With Lynch Syndrome Park SS, Chan M, Velaiutham S, Vargas AC 10.1177/10668969241226704
38297350 Rare germline mutation and MSH2-&MSH6 + expression in a double primary carcinomaof colorectal carcinoma and endometrial carcinoma: a case report Zhang T, Huang X, ..., Che S 10.1186/s13000-024-01447-8
38423221 Colorectal neuroendocrine carcinoma and mixed neuroendocrine-non-neuroendocrineneoplasm: Prognostic factors and PD-L1 expression Ho YH, Hsu CY, Yau Li AF, Liang WY 10.1016/j.humpath.2024.02.012
38362598 Integrated analyses of the genetic and clinicopathological features ofcholangiolocarcinoma: cholangiolocarcinoma may be characterized bymismatch-repair deficiency Makino K, Ishii T, ..., Hatano E 10.1002/path.6257
38298064 Development of Complementary Photo-arginine/lysine to Promote Discovery ofArg/Lys hPTMs Interactomes Zong Y, Weiss N, ..., Huang J 10.1002/advs.202307526
38395750 Association between colorectal cancer, the frequency of Bacteroides fragilis, andthe level of mismatch repair genes expression in the biopsy samples of Iranianpatients Nazarinejad N, Hajikhani B, ..., Dadashi M 10.1186/s12876-024-03169-z
38415639 Enterohemorrhagic Escherichia coli effector EspF triggers oxidative DNA lesionsin intestinal epithelial cells Fang Y, Fu M, ..., Wan C 10.1128/iai.00001-24
38315739 Nonhomologous tails direct heteroduplex rejection and mismatch correction duringsingle-strand annealing in Saccharomyces cerevisiae Sapede E, Sugawara N, ..., Haber JE 10.1371/journal.pgen.1010527
38383663 Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynchsyndrome Dalene Skarping K, Arning L, ..., Gebre-Medhin S 10.1038/s41598-024-54277-5
38401766 Plant-specific environmental and developmental signals regulate the mismatchrepair protein MSH6 in Arabidopsis thaliana Gonzalez V, Figueroa NR, Spampinato CP 10.1016/j.plantsci.2024.112050
38416847 Familial Intraductal Papillary Mucinous Neoplasm Associated With the GermlineMSH6 Missense Variant and Progression of Pancreatic cancer Tezuka K, Yamakawa M, ..., Motoi F 10.1097/MPA.0000000000002313
38302727 The new 2023 F IGO staging system for endometrial cancer: what is different fromthe previous 2009 F IGO staging system? Han KH, Park N, ..., Kim H 10.3802/jgo.2024.35.e59
38295361 Extra-Ocular Sebaceous Carcinoma in Situ of the Arm of an Elder Male: An UnusualPresentation in an Atypical Location Shaker N, Sangueza OP, Shaker N, Pradhan D 10.1177/10668969241226701
38295319 Feasibility and Clinical Utility of Reporting Hereditary Cancer PredispositionPathogenic Variants Identified in Research Germline Sequencing: A ProspectiveInterventional Study Hutchcraft ML, Zhang S, ..., Kolesar JM 10.1200/PO.23.00266