Mitochondrial protein, outer mitochondrial membrane proteome 37 (POMP37) Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 6 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005741 | mitochondrial outer membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019867 | outer membrane | 3 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
GO:0031968 | organelle outer membrane | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4I4S0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016829 | lyase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.732 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 508 | 510 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.492 |
CLV_Separin_Metazoa | 219 | 223 | PF03568 | 0.456 |
DEG_APCC_DBOX_1 | 427 | 435 | PF00400 | 0.388 |
DEG_APCC_DBOX_1 | 596 | 604 | PF00400 | 0.247 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.648 |
DOC_CKS1_1 | 356 | 361 | PF01111 | 0.301 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 213 | 225 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 434 | 440 | PF00134 | 0.435 |
DOC_CYCLIN_yCln2_LP_2 | 573 | 579 | PF00134 | 0.446 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 40 | 47 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 613 | 623 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 99 | 110 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 616 | 625 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.446 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.353 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.632 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.388 |
DOC_USP7_UBL2_3 | 527 | 531 | PF12436 | 0.416 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 100 | 110 | PF00244 | 0.508 |
LIG_Actin_WH2_2 | 255 | 272 | PF00022 | 0.411 |
LIG_APCC_ABBA_1 | 471 | 476 | PF00400 | 0.446 |
LIG_APCC_ABBA_1 | 583 | 588 | PF00400 | 0.437 |
LIG_BIR_III_4 | 125 | 129 | PF00653 | 0.649 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.579 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.506 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.639 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.495 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.527 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.500 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.393 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.346 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.461 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.427 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 283 | 287 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 46 | 50 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 461 | 472 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 441 | 445 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.415 |
LIG_PDZ_Class_2 | 635 | 640 | PF00595 | 0.485 |
LIG_Pex14_1 | 291 | 295 | PF04695 | 0.347 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.425 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.385 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.316 |
LIG_SH2_GRB2like | 309 | 312 | PF00017 | 0.331 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.399 |
LIG_SH3_1 | 270 | 276 | PF00018 | 0.422 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.542 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.429 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.563 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.382 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.355 |
LIG_SUMO_SIM_anti_2 | 257 | 263 | PF11976 | 0.565 |
LIG_SUMO_SIM_anti_2 | 619 | 625 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 104 | 111 | PF11976 | 0.632 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 606 | 612 | PF11976 | 0.466 |
LIG_TRAF2_1 | 564 | 567 | PF00917 | 0.374 |
LIG_TRFH_1 | 464 | 468 | PF08558 | 0.446 |
LIG_TYR_ITIM | 440 | 445 | PF00017 | 0.312 |
MOD_CDC14_SPxK_1 | 575 | 578 | PF00782 | 0.446 |
MOD_CDK_SPK_2 | 243 | 248 | PF00069 | 0.570 |
MOD_CDK_SPxK_1 | 572 | 578 | PF00069 | 0.446 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.528 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.710 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.465 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.367 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.549 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.580 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.638 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.518 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.458 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.362 |
MOD_Cter_Amidation | 524 | 527 | PF01082 | 0.525 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.815 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.466 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.588 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.455 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.704 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.450 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.404 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.409 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.737 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.402 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.472 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.438 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.646 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.381 |
MOD_N-GLC_1 | 633 | 638 | PF02516 | 0.418 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.603 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.365 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.563 |
MOD_NEK2_2 | 535 | 540 | PF00069 | 0.329 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.453 |
MOD_PKA_1 | 543 | 549 | PF00069 | 0.331 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.421 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.351 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.430 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.759 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.559 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.520 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.472 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.353 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.572 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.464 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.366 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.459 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.492 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.442 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.572 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.704 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.536 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.297 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.572 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.395 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 216 | 219 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 230 | 238 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 320 | 325 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 502 | 510 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 78 | 88 | PF00179 | 0.552 |
TRG_DiLeu_BaEn_1 | 619 | 624 | PF01217 | 0.301 |
TRG_DiLeu_BaEn_2 | 469 | 475 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 598 | 603 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.515 |
TRG_NES_CRM1_1 | 146 | 158 | PF08389 | 0.503 |
TRG_NLS_Bipartite_1 | 526 | 546 | PF00514 | 0.247 |
TRG_NLS_MonoExtN_4 | 540 | 546 | PF00514 | 0.437 |
TRG_NLS_MonoExtN_4 | 597 | 602 | PF00514 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 509 | 514 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 601 | 606 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3W3 | Leptomonas seymouri | 61% | 100% |
A0A0S4JNB4 | Bodo saltans | 22% | 100% |
A0A1X0P222 | Trypanosomatidae | 22% | 100% |
A0A3Q8IFG9 | Leishmania donovani | 99% | 100% |
A0A3Q8IHT6 | Leishmania donovani | 25% | 100% |
A0A3R7LIT5 | Trypanosoma rangeli | 32% | 100% |
A4HHL0 | Leishmania braziliensis | 78% | 100% |
A4I5C4 | Leishmania infantum | 25% | 100% |
C9ZQQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
C9ZUB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 92% |
E9AE72 | Leishmania major | 94% | 100% |
E9ALL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B0M2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q7L0 | Leishmania major | 25% | 100% |