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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 14 |
GO:0032991 | protein-containing complex | 1 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043228 | non-membrane-bounded organelle | 3 | 14 |
GO:0043229 | intracellular organelle | 3 | 14 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:1990904 | ribonucleoprotein complex | 2 | 14 |
GO:0035869 | ciliary transition zone | 2 | 2 |
Related structures:
AlphaFold database: A4HLH8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.469 |
CLV_PCSK_FUR_1 | 75 | 79 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.510 |
CLV_Separin_Metazoa | 427 | 431 | PF03568 | 0.570 |
DEG_APCC_DBOX_1 | 373 | 381 | PF00400 | 0.440 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.597 |
DEG_SIAH_1 | 590 | 598 | PF03145 | 0.499 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.465 |
DOC_MAPK_DCC_7 | 467 | 477 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 6 | 14 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 357 | 364 | PF00069 | 0.348 |
DOC_MAPK_NFAT4_5 | 357 | 365 | PF00069 | 0.343 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.600 |
DOC_PP2B_LxvP_1 | 470 | 473 | PF13499 | 0.740 |
DOC_PP2B_LxvP_1 | 511 | 514 | PF13499 | 0.602 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.749 |
DOC_PP2B_LxvP_1 | 562 | 565 | PF13499 | 0.613 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.725 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 536 | 540 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.498 |
LIG_14-3-3_CterR_2 | 630 | 634 | PF00244 | 0.719 |
LIG_Actin_WH2_2 | 239 | 256 | PF00022 | 0.521 |
LIG_APCC_ABBA_1 | 106 | 111 | PF00400 | 0.472 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.344 |
LIG_Clathr_ClatBox_1 | 578 | 582 | PF01394 | 0.533 |
LIG_EVH1_1 | 511 | 515 | PF00568 | 0.541 |
LIG_EVH1_1 | 562 | 566 | PF00568 | 0.631 |
LIG_EVH1_2 | 563 | 567 | PF00568 | 0.510 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.493 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.649 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.467 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.458 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.463 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.645 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.542 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.667 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.654 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.620 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.609 |
LIG_GBD_Chelix_1 | 279 | 287 | PF00786 | 0.429 |
LIG_Integrin_RGD_1 | 133 | 135 | PF01839 | 0.404 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.413 |
LIG_LIR_LC3C_4 | 361 | 364 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.733 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.479 |
LIG_LYPXL_SIV_4 | 344 | 352 | PF13949 | 0.586 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.524 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.493 |
LIG_SH2_SRC | 555 | 558 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.539 |
LIG_SH3_1 | 444 | 450 | PF00018 | 0.593 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.666 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.693 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.678 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.665 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.649 |
LIG_SH3_3 | 515 | 521 | PF00018 | 0.678 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.664 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.597 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.524 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.577 |
LIG_SUMO_SIM_anti_2 | 425 | 430 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 361 | 367 | PF11976 | 0.458 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.520 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.520 |
LIG_WW_2 | 447 | 450 | PF00397 | 0.478 |
LIG_WW_3 | 496 | 500 | PF00397 | 0.583 |
LIG_WW_3 | 539 | 543 | PF00397 | 0.520 |
MOD_CDC14_SPxK_1 | 539 | 542 | PF00782 | 0.517 |
MOD_CDK_SPxK_1 | 536 | 542 | PF00069 | 0.525 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.704 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.351 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.572 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.503 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.449 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.509 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.544 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.711 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.729 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.738 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.597 |
MOD_DYRK1A_RPxSP_1 | 536 | 540 | PF00069 | 0.524 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.505 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.460 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.301 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.509 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.504 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.433 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.367 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.409 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.413 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.511 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.418 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.532 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.624 |
MOD_GlcNHglycan | 482 | 486 | PF01048 | 0.692 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.622 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.695 |
MOD_GlcNHglycan | 582 | 586 | PF01048 | 0.644 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.459 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.392 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.504 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.586 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.486 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.477 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.489 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.426 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.797 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.684 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.728 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.575 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.669 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.355 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.287 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.272 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.518 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.452 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.430 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.430 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.763 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.425 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.380 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.474 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.633 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.541 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.723 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.563 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.311 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.554 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.545 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.493 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.636 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.825 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.527 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.354 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.421 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.492 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.486 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.409 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.452 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.479 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.648 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.491 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.513 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.628 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.424 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.611 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.661 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 19 | 29 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 416 | 423 | PF00179 | 0.622 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.579 |
TRG_DiLeu_BaEn_1 | 358 | 363 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 152 | 157 | PF01217 | 0.306 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 630 | 632 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.651 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I367 | Leptomonas seymouri | 70% | 93% |
A0A0S4JA89 | Bodo saltans | 35% | 72% |
A0A1X0P0X2 | Trypanosomatidae | 39% | 96% |
A0A1X0P178 | Trypanosomatidae | 36% | 100% |
A0A3Q8IGU1 | Leishmania donovani | 74% | 100% |
A0A3R7M637 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X6R5 | Leishmania donovani | 29% | 73% |
A4HLH9 | Leishmania braziliensis | 31% | 82% |
A4I8Y8 | Leishmania infantum | 74% | 100% |
A4I8Y9 | Leishmania infantum | 28% | 74% |
D0A4Y6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 86% |
E9B3V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9B3V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 72% |
Q4Q466 | Leishmania major | 28% | 74% |
Q4Q467 | Leishmania major | 74% | 96% |