Homologous to yeast mitochondrial OMS1 methyltransferase, but many Kinetoplastid homologs lack the transit signal.. One sub-group of these proteins have an N-terminal membrane anchor, while others might possess an internal Tm segment potentially targeted to mitochondria.. Localization: Mitochondrial (by homology) / Others (by feature)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HMH8
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 2 |
GO:0032259 | methylation | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.440 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.587 |
DOC_MAPK_gen_1 | 276 | 285 | PF00069 | 0.203 |
DOC_MAPK_gen_1 | 315 | 325 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.240 |
DOC_PP4_FxxP_1 | 96 | 99 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.631 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.586 |
DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.342 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.264 |
LIG_14-3-3_CanoR_1 | 264 | 273 | PF00244 | 0.240 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.239 |
LIG_AP2alpha_1 | 339 | 343 | PF02296 | 0.264 |
LIG_APCC_ABBA_1 | 283 | 288 | PF00400 | 0.182 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.613 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.580 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.637 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.259 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.679 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.368 |
LIG_LIR_Gen_1 | 288 | 298 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.258 |
LIG_LYPXL_SIV_4 | 332 | 340 | PF13949 | 0.250 |
LIG_LYPXL_yS_3 | 333 | 336 | PF13949 | 0.264 |
LIG_LYPXL_yS_3 | 388 | 391 | PF13949 | 0.303 |
LIG_PCNA_yPIPBox_3 | 355 | 364 | PF02747 | 0.239 |
LIG_Pex14_1 | 158 | 162 | PF04695 | 0.562 |
LIG_Pex14_1 | 338 | 342 | PF04695 | 0.244 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.437 |
LIG_Pex14_2 | 339 | 343 | PF04695 | 0.240 |
LIG_PTB_Apo_2 | 373 | 380 | PF02174 | 0.295 |
LIG_PTB_Phospho_1 | 373 | 379 | PF10480 | 0.299 |
LIG_REV1ctd_RIR_1 | 199 | 207 | PF16727 | 0.451 |
LIG_RPA_C_Fungi | 363 | 375 | PF08784 | 0.327 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.276 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.276 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.430 |
LIG_SH2_STAT3 | 342 | 345 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.336 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.399 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.290 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.290 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.304 |
LIG_SUMO_SIM_anti_2 | 8 | 15 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 320 | 327 | PF11976 | 0.316 |
LIG_TYR_ITIM | 386 | 391 | PF00017 | 0.343 |
LIG_TYR_ITSM | 379 | 386 | PF00017 | 0.316 |
MOD_CDC14_SPxK_1 | 358 | 361 | PF00782 | 0.309 |
MOD_CDK_SPxK_1 | 355 | 361 | PF00069 | 0.309 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.515 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.524 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.660 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.290 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.454 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.290 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.728 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.548 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.510 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.488 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.531 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.513 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.523 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.743 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.568 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.326 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.290 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.306 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.407 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.360 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.508 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.419 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.651 |
MOD_Plk_2-3 | 397 | 403 | PF00069 | 0.399 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.344 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.498 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.360 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.611 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.280 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.309 |
MOD_SUMO_rev_2 | 366 | 374 | PF00179 | 0.290 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.360 |
TRG_NLS_MonoExtC_3 | 275 | 281 | PF00514 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 210 | 214 | PF00026 | 0.282 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I341 | Leptomonas seymouri | 76% | 100% |
A0A0S4J626 | Bodo saltans | 64% | 100% |
A0A1X0P6L5 | Trypanosomatidae | 75% | 100% |
A0A3Q8IIX0 | Leishmania donovani | 90% | 100% |
A0A422NQ76 | Trypanosoma rangeli | 72% | 100% |
A4IB48 | Leishmania infantum | 93% | 100% |
A4IB58 | Leishmania infantum | 90% | 100% |
C9ZZG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 100% |
E9AEX9 | Leishmania major | 90% | 100% |
E9B635 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DKE6 | Trypanosoma cruzi | 68% | 100% |