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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H8M0
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_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.488 |
CLV_PCSK_FUR_1 | 69 | 73 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 291 | 297 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.282 |
DEG_APCC_KENBOX_2 | 142 | 146 | PF00400 | 0.434 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.669 |
DEG_SPOP_SBC_1 | 131 | 135 | PF00917 | 0.306 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.365 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.389 |
DOC_CYCLIN_RxL_1 | 325 | 333 | PF00134 | 0.181 |
DOC_MAPK_gen_1 | 112 | 120 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 392 | 402 | PF00069 | 0.236 |
DOC_MAPK_gen_1 | 41 | 50 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.239 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.284 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.249 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.340 |
DOC_USP7_MATH_2 | 335 | 341 | PF00917 | 0.181 |
DOC_USP7_UBL2_3 | 395 | 399 | PF12436 | 0.331 |
DOC_USP7_UBL2_3 | 449 | 453 | PF12436 | 0.347 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 307 | 311 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 323 | 341 | PF00022 | 0.181 |
LIG_APCC_ABBAyCdc20_2 | 216 | 222 | PF00400 | 0.338 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.367 |
LIG_Clathr_ClatBox_1 | 400 | 404 | PF01394 | 0.249 |
LIG_CtBP_PxDLS_1 | 335 | 339 | PF00389 | 0.282 |
LIG_deltaCOP1_diTrp_1 | 448 | 455 | PF00928 | 0.392 |
LIG_deltaCOP1_diTrp_1 | 470 | 475 | PF00928 | 0.374 |
LIG_DLG_GKlike_1 | 41 | 48 | PF00625 | 0.411 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.327 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.279 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.302 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.427 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 174 | 179 | PF02991 | 0.339 |
LIG_LIR_Apic_2 | 379 | 383 | PF02991 | 0.236 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 470 | 477 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.444 |
LIG_PCNA_yPIPBox_3 | 426 | 440 | PF02747 | 0.236 |
LIG_PDZ_Class_1 | 483 | 488 | PF00595 | 0.487 |
LIG_PTB_Apo_2 | 92 | 99 | PF02174 | 0.327 |
LIG_PTB_Phospho_1 | 92 | 98 | PF10480 | 0.329 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.181 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 136 | 139 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.325 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.429 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.235 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.236 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.227 |
LIG_SH3_4 | 395 | 402 | PF00018 | 0.331 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.236 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.439 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.424 |
LIG_UBA3_1 | 137 | 143 | PF00899 | 0.446 |
LIG_UBA3_1 | 400 | 407 | PF00899 | 0.236 |
LIG_WRC_WIRS_1 | 377 | 382 | PF05994 | 0.249 |
LIG_WW_1 | 31 | 34 | PF00397 | 0.392 |
MOD_CDK_SPxK_1 | 171 | 177 | PF00069 | 0.342 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.411 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.352 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.373 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.390 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.422 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.477 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.348 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.229 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.322 |
MOD_CMANNOS | 428 | 431 | PF00535 | 0.436 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.678 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.548 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.411 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.591 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.718 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.643 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.606 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.477 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.531 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.498 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.366 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.527 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.259 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.272 |
MOD_LATS_1 | 405 | 411 | PF00433 | 0.331 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.653 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.486 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.282 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.299 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.549 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.181 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.292 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.298 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.500 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.536 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.328 |
MOD_PK_1 | 407 | 413 | PF00069 | 0.246 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.456 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.496 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.263 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.331 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.267 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.336 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.471 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.263 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.262 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.244 |
MOD_Plk_2-3 | 221 | 227 | PF00069 | 0.500 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.272 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.449 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.365 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.487 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.342 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.388 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 165 | 168 | PF00179 | 0.243 |
MOD_SUMO_rev_2 | 446 | 455 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 49 | 58 | PF00179 | 0.331 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.267 |
TRG_DiLeu_BaEn_2 | 236 | 242 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_3 | 305 | 311 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_4 | 237 | 243 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 268 | 273 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.249 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.282 |
TRG_NLS_MonoCore_2 | 213 | 218 | PF00514 | 0.477 |
TRG_NLS_MonoExtN_4 | 214 | 219 | PF00514 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 271 | 276 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8I0 | Leptomonas seymouri | 73% | 100% |
A0A1X0NZ02 | Trypanosomatidae | 46% | 100% |
A0A3Q8I9F7 | Leishmania donovani | 86% | 100% |
A0A3R7NGZ3 | Trypanosoma rangeli | 47% | 100% |
A4HWZ1 | Leishmania infantum | 85% | 100% |
C9ZW11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AQQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QES4 | Leishmania major | 85% | 100% |
V5ANK2 | Trypanosoma cruzi | 47% | 100% |