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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ARJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.594 |
CLV_PCSK_FUR_1 | 247 | 251 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.365 |
DEG_APCC_DBOX_1 | 238 | 246 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.321 |
DEG_MDM2_SWIB_1 | 382 | 390 | PF02201 | 0.464 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.637 |
DEG_SCF_FBW7_1 | 377 | 384 | PF00400 | 0.478 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.671 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.495 |
DOC_CYCLIN_RxL_1 | 244 | 257 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 244 | 254 | PF00069 | 0.504 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.321 |
DOC_PP4_MxPP_1 | 131 | 134 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.658 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.544 |
DOC_USP7_UBL2_3 | 476 | 480 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.511 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.512 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.658 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.411 |
LIG_LIR_Apic_2 | 268 | 272 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 511 | 517 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 597 | 602 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 48 | 56 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 574 | 580 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 574 | 579 | PF02991 | 0.321 |
LIG_LYPXL_S_1 | 157 | 161 | PF13949 | 0.513 |
LIG_LYPXL_yS_3 | 158 | 161 | PF13949 | 0.660 |
LIG_Pex14_2 | 382 | 386 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 376 | 383 | PF02174 | 0.495 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.548 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.640 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.411 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 295 | 299 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.722 |
LIG_SH2_PTP2 | 181 | 184 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 5 | 8 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.321 |
LIG_SH3_1 | 5 | 11 | PF00018 | 0.616 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.651 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.713 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.539 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.643 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.638 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.683 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.430 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.797 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.458 |
LIG_SxIP_EBH_1 | 353 | 363 | PF03271 | 0.598 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.595 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.630 |
LIG_WRC_WIRS_1 | 448 | 453 | PF05994 | 0.321 |
LIG_WW_1 | 46 | 49 | PF00397 | 0.616 |
LIG_WW_2 | 438 | 441 | PF00397 | 0.566 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.643 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.721 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.735 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.613 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.676 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.646 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.321 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.679 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.373 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.411 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.625 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.321 |
MOD_Cter_Amidation | 518 | 521 | PF01082 | 0.321 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.670 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.720 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.518 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.539 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.592 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.630 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.633 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.617 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.503 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.493 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.739 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.321 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.511 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.641 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.669 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.716 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.713 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.670 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.718 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.522 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.605 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.702 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.494 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.390 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.624 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.599 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.330 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.676 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.586 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.505 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.488 |
MOD_N-GLC_1 | 597 | 602 | PF02516 | 0.344 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.720 |
MOD_N-GLC_2 | 570 | 572 | PF02516 | 0.321 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.620 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.321 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.375 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.299 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.734 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.512 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.516 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.658 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.525 |
MOD_PKA_1 | 498 | 504 | PF00069 | 0.625 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.735 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.520 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.738 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.362 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.411 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.321 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.328 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.735 |
MOD_Plk_2-3 | 562 | 568 | PF00069 | 0.321 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.524 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.321 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.735 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.709 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.556 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.639 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.793 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.321 |
MOD_SUMO_for_1 | 547 | 550 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 492 | 501 | PF00179 | 0.710 |
MOD_SUMO_rev_2 | 622 | 627 | PF00179 | 0.453 |
TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.637 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.609 |
TRG_NES_CRM1_1 | 243 | 257 | PF08389 | 0.507 |
TRG_NLS_MonoExtC_3 | 627 | 632 | PF00514 | 0.585 |
TRG_NLS_MonoExtN_4 | 625 | 632 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 250 | 255 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2D5 | Leptomonas seymouri | 55% | 100% |
A0A3Q8I9Y5 | Leishmania donovani | 89% | 100% |
A4H9G8 | Leishmania braziliensis | 78% | 99% |
A4HXT6 | Leishmania infantum | 89% | 100% |
Q4QDY1 | Leishmania major | 89% | 98% |