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 | 1 |
GO:0016020 | membrane | 2 | 4 |
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 | 4 |
Related structures:
AlphaFold database: A0A3S7X9K3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.441 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.582 |
DEG_SPOP_SBC_1 | 527 | 531 | PF00917 | 0.635 |
DOC_ANK_TNKS_1 | 237 | 244 | PF00023 | 0.728 |
DOC_MAPK_DCC_7 | 49 | 57 | PF00069 | 0.666 |
DOC_MAPK_gen_1 | 313 | 322 | PF00069 | 0.743 |
DOC_MAPK_HePTP_8 | 310 | 322 | PF00069 | 0.748 |
DOC_MAPK_MEF2A_6 | 313 | 322 | PF00069 | 0.748 |
DOC_MAPK_MEF2A_6 | 361 | 369 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.625 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.705 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.655 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.641 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.766 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 33 | 40 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 550 | 556 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 559 | 564 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.408 |
LIG_APCC_ABBAyCdc20_2 | 539 | 545 | PF00400 | 0.583 |
LIG_deltaCOP1_diTrp_1 | 573 | 582 | PF00928 | 0.638 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.414 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.688 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.657 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.353 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.650 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.734 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.669 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.572 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.500 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.620 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.719 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.773 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.753 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.745 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.667 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.642 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.591 |
LIG_GBD_Chelix_1 | 44 | 52 | PF00786 | 0.483 |
LIG_LIR_Apic_2 | 390 | 396 | PF02991 | 0.673 |
LIG_LIR_Apic_2 | 441 | 447 | PF02991 | 0.687 |
LIG_LIR_Apic_2 | 554 | 558 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 198 | 204 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 501 | 506 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 472 | 478 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.617 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.694 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.689 |
LIG_Pex14_2 | 449 | 453 | PF04695 | 0.643 |
LIG_PTB_Apo_2 | 512 | 519 | PF02174 | 0.598 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.603 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.710 |
LIG_SH2_NCK_1 | 218 | 222 | PF00017 | 0.603 |
LIG_SH2_NCK_1 | 393 | 397 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.706 |
LIG_SH2_PTP2 | 555 | 558 | PF00017 | 0.552 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.632 |
LIG_SH3_2 | 343 | 348 | PF14604 | 0.726 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.766 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.764 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.655 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.672 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.648 |
LIG_SUMO_SIM_anti_2 | 219 | 226 | PF11976 | 0.660 |
LIG_SUMO_SIM_anti_2 | 562 | 567 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 219 | 226 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 363 | 368 | PF11976 | 0.696 |
LIG_TYR_ITIM | 473 | 478 | PF00017 | 0.583 |
MOD_CDK_SPK_2 | 484 | 489 | PF00069 | 0.650 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.745 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.749 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.779 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.676 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.761 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.808 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.800 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.656 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.653 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.576 |
MOD_Cter_Amidation | 188 | 191 | PF01082 | 0.553 |
MOD_Cter_Amidation | 246 | 249 | PF01082 | 0.626 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.564 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.382 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.533 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.612 |
MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.567 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.478 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.501 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.500 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.467 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.520 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.485 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.462 |
MOD_GlcNHglycan | 534 | 538 | PF01048 | 0.367 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.556 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.344 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.764 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.681 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.731 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.788 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.738 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.692 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.799 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.686 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.666 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.623 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.617 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.787 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.520 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.654 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.733 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.675 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.707 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.601 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.703 |
MOD_OFUCOSY | 332 | 337 | PF10250 | 0.435 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.804 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.765 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.596 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.682 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.678 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.612 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.625 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.734 |
MOD_PKB_1 | 248 | 256 | PF00069 | 0.802 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.761 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.310 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.545 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.717 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.662 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.668 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.691 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.668 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.617 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.745 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.770 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.757 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.648 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 177 | 183 | PF00179 | 0.684 |
MOD_SUMO_rev_2 | 356 | 363 | PF00179 | 0.690 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.716 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.590 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVZ7 | Leptomonas seymouri | 46% | 94% |
A0A3R7NG87 | Trypanosoma rangeli | 28% | 100% |
A4HMX8 | Leishmania braziliensis | 70% | 100% |
A4IBK2 | Leishmania infantum | 98% | 100% |
C9ZZ42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AFD5 | Leishmania major | 89% | 100% |
E9B6J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5DUQ9 | Trypanosoma cruzi | 23% | 100% |