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: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005741 | mitochondrial outer membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 5 |
GO:0019867 | outer membrane | 3 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031966 | mitochondrial membrane | 4 | 2 |
GO:0031968 | organelle outer membrane | 4 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AFD5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.676 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.422 |
CLV_PCSK_PC7_1 | 28 | 34 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.354 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.464 |
DEG_SPOP_SBC_1 | 531 | 535 | PF00917 | 0.557 |
DOC_ANK_TNKS_1 | 112 | 119 | PF00023 | 0.606 |
DOC_ANK_TNKS_1 | 241 | 248 | PF00023 | 0.664 |
DOC_MAPK_DCC_7 | 53 | 61 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.667 |
DOC_MAPK_HePTP_8 | 314 | 326 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 317 | 326 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 365 | 373 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 53 | 61 | PF00069 | 0.595 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.624 |
DOC_PP4_FxxP_1 | 341 | 344 | PF00568 | 0.794 |
DOC_PP4_FxxP_1 | 397 | 400 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.714 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.830 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 104 | 111 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 338 | 344 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 352 | 361 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 554 | 560 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 563 | 568 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.297 |
LIG_BRCT_BRCA1_1 | 393 | 397 | PF00533 | 0.600 |
LIG_deltaCOP1_diTrp_1 | 577 | 586 | PF00928 | 0.602 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.355 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.569 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.621 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.525 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.716 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.663 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.510 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.501 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.575 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.686 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.755 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.689 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.667 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.640 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.605 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.580 |
LIG_GBD_Chelix_1 | 48 | 56 | PF00786 | 0.403 |
LIG_HP1_1 | 284 | 288 | PF01393 | 0.556 |
LIG_LIR_Apic_2 | 394 | 400 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 445 | 451 | PF02991 | 0.664 |
LIG_LIR_Apic_2 | 558 | 562 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 202 | 208 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 391 | 400 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 505 | 510 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.570 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.655 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.610 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.502 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.619 |
LIG_PTB_Apo_2 | 516 | 523 | PF02174 | 0.520 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.508 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.644 |
LIG_SH2_NCK_1 | 222 | 226 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 448 | 451 | PF00017 | 0.617 |
LIG_SH2_PTP2 | 559 | 562 | PF00017 | 0.499 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.573 |
LIG_SH2_SRC | 65 | 68 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.602 |
LIG_SH3_2 | 347 | 352 | PF14604 | 0.652 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.633 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.678 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.725 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.653 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.609 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.646 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.593 |
LIG_SUMO_SIM_anti_2 | 223 | 230 | PF11976 | 0.624 |
LIG_SUMO_SIM_anti_2 | 367 | 372 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 284 | 291 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.615 |
LIG_TYR_ITIM | 477 | 482 | PF00017 | 0.538 |
LIG_WRC_WIRS_1 | 370 | 375 | PF05994 | 0.667 |
MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.582 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.669 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.734 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.577 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.650 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.660 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.718 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.782 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.630 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.621 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.565 |
MOD_Cter_Amidation | 192 | 195 | PF01082 | 0.470 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.525 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.468 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.390 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.558 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.611 |
MOD_GlcNHglycan | 248 | 252 | PF01048 | 0.540 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.471 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.449 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.453 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.463 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.471 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.352 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.591 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.661 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.750 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.630 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.720 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.834 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.612 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.730 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.665 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.571 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.599 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.606 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.755 |
MOD_N-GLC_1 | 547 | 552 | PF02516 | 0.271 |
MOD_N-GLC_2 | 334 | 336 | PF02516 | 0.358 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.603 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.693 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.630 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.701 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.569 |
MOD_NEK2_2 | 328 | 333 | PF00069 | 0.600 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.716 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.661 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.625 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.636 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.504 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.567 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.642 |
MOD_PKB_1 | 252 | 260 | PF00069 | 0.714 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.634 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.497 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.566 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.659 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.652 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.638 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.651 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.619 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.609 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.627 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.830 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.565 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.574 |
MOD_SUMO_rev_2 | 358 | 367 | PF00179 | 0.614 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.654 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.241 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVZ7 | Leptomonas seymouri | 45% | 94% |
A0A3R7NG87 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X9K3 | Leishmania donovani | 89% | 100% |
A4HMX8 | Leishmania braziliensis | 70% | 100% |
A4IBK2 | Leishmania infantum | 89% | 100% |
C9ZZ42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B6J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5DUQ9 | Trypanosoma cruzi | 23% | 100% |