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: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AZL1
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0030544 | Hsp70 protein binding | 4 | 12 |
GO:0031072 | heat shock protein binding | 3 | 12 |
GO:0051879 | Hsp90 protein binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.706 |
CLV_MEL_PAP_1 | 602 | 608 | PF00089 | 0.515 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.515 |
CLV_PCSK_FUR_1 | 332 | 336 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.465 |
CLV_Separin_Metazoa | 670 | 674 | PF03568 | 0.521 |
DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.684 |
DEG_COP1_1 | 22 | 30 | PF00400 | 0.684 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.551 |
DEG_SPOP_SBC_1 | 159 | 163 | PF00917 | 0.525 |
DOC_ANK_TNKS_1 | 640 | 647 | PF00023 | 0.487 |
DOC_CYCLIN_RxL_1 | 314 | 324 | PF00134 | 0.437 |
DOC_CYCLIN_RxL_1 | 411 | 419 | PF00134 | 0.580 |
DOC_CYCLIN_RxL_1 | 549 | 558 | PF00134 | 0.249 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.641 |
DOC_MAPK_gen_1 | 332 | 341 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 458 | 467 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 586 | 594 | PF00069 | 0.348 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.665 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.648 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.643 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 129 | 138 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 247 | 256 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 504 | 514 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 521 | 527 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 605 | 613 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 689 | 694 | PF00244 | 0.476 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.483 |
LIG_APCC_ABBA_1 | 577 | 582 | PF00400 | 0.476 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 563 | 567 | PF00533 | 0.404 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.456 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.418 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.356 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.536 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.489 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.447 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.428 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.391 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.551 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.781 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.722 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.621 |
LIG_FHA_2 | 665 | 671 | PF00498 | 0.527 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.529 |
LIG_Integrin_isoDGR_2 | 384 | 386 | PF01839 | 0.442 |
LIG_LIR_Apic_2 | 78 | 84 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 558 | 567 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 576 | 584 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 60 | 67 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 94 | 105 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 597 | 602 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 703 | 709 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.525 |
LIG_RPA_C_Fungi | 247 | 259 | PF08784 | 0.485 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.678 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.474 |
LIG_SH2_CRK | 560 | 564 | PF00017 | 0.384 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.496 |
LIG_SH2_GRB2like | 233 | 236 | PF00017 | 0.498 |
LIG_SH2_SRC | 343 | 346 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.478 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.588 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.459 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.544 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.541 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.503 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.534 |
LIG_TRAF2_1 | 484 | 487 | PF00917 | 0.534 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.458 |
LIG_TRAF2_1 | 697 | 700 | PF00917 | 0.424 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.453 |
LIG_WRC_WIRS_1 | 678 | 683 | PF05994 | 0.557 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.677 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.617 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.344 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.393 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.615 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.403 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.351 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.398 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.604 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.689 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.502 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.416 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.454 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.542 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.552 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.450 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.710 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.703 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.557 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.405 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.486 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.519 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.409 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.455 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.673 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.349 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.452 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.424 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.555 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.438 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.499 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.638 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.734 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.342 |
MOD_N-GLC_1 | 664 | 669 | PF02516 | 0.529 |
MOD_N-GLC_2 | 664 | 666 | PF02516 | 0.504 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.439 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.677 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.347 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.493 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.433 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.410 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.392 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.561 |
MOD_NEK2_2 | 130 | 135 | PF00069 | 0.680 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.432 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.384 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.438 |
MOD_PK_1 | 588 | 594 | PF00069 | 0.390 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.520 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.507 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.534 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.477 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.441 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.459 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.561 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.663 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.527 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.538 |
MOD_Plk_1 | 625 | 631 | PF00069 | 0.506 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.700 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.528 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.407 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.610 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.334 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.519 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.373 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.452 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.514 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.472 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.557 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.644 |
MOD_SUMO_for_1 | 697 | 700 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 121 | 125 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 656 | 661 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 371 | 376 | PF01217 | 0.293 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.677 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 688 | 691 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.668 |
TRG_NLS_MonoExtC_3 | 333 | 338 | PF00514 | 0.446 |
TRG_NLS_MonoExtN_4 | 332 | 338 | PF00514 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 470 | 474 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I228 | Leptomonas seymouri | 70% | 100% |
A0A0S4JB35 | Bodo saltans | 29% | 96% |
A0A1X0NZW8 | Trypanosomatidae | 30% | 92% |
A0A3Q8IAV8 | Leishmania donovani | 95% | 100% |
A0A3R7KXE4 | Trypanosoma rangeli | 32% | 100% |
A4HG90 | Leishmania braziliensis | 85% | 100% |
A4I3C4 | Leishmania infantum | 95% | 100% |
D0A822 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 97% |
Q4Q8M0 | Leishmania major | 94% | 100% |
V5DH70 | Trypanosoma cruzi | 31% | 95% |