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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HHF3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.678 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 350 | 352 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.377 |
DEG_ODPH_VHL_1 | 521 | 534 | PF01847 | 0.525 |
DEG_SPOP_SBC_1 | 364 | 368 | PF00917 | 0.579 |
DEG_SPOP_SBC_1 | 608 | 612 | PF00917 | 0.541 |
DOC_MAPK_gen_1 | 200 | 211 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.541 |
DOC_MAPK_NFAT4_5 | 234 | 242 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 280 | 287 | PF00149 | 0.577 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.783 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.708 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.661 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 222 | 229 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 363 | 373 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 574 | 580 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.690 |
LIG_Actin_WH2_2 | 339 | 356 | PF00022 | 0.484 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.577 |
LIG_APCC_ABBA_1 | 286 | 291 | PF00400 | 0.400 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 144 | 148 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.514 |
LIG_deltaCOP1_diTrp_1 | 490 | 500 | PF00928 | 0.523 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.577 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.577 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.519 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.567 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.655 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.611 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.577 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.602 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.547 |
LIG_IBAR_NPY_1 | 637 | 639 | PF08397 | 0.700 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 496 | 505 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.664 |
LIG_PTB_Apo_2 | 638 | 645 | PF02174 | 0.500 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.556 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.527 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.701 |
LIG_SH2_GRB2like | 639 | 642 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.700 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.664 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.693 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.500 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.603 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.570 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.584 |
MOD_CDK_SPK_2 | 624 | 629 | PF00069 | 0.659 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.745 |
MOD_CDK_SPxxK_3 | 382 | 389 | PF00069 | 0.511 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.561 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.598 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.604 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.679 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.569 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.522 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.576 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.519 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.593 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.545 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.736 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.728 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.679 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.615 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.556 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.577 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.607 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.545 |
MOD_DYRK1A_RPxSP_1 | 20 | 24 | PF00069 | 0.556 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.377 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.782 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.483 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.728 |
MOD_GlcNHglycan | 499 | 503 | PF01048 | 0.589 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.519 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.630 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.583 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.752 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.580 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.597 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.720 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.654 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.668 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.712 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.627 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.654 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.640 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.553 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.670 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.725 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.471 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.593 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.681 |
MOD_N-GLC_1 | 640 | 645 | PF02516 | 0.500 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.727 |
MOD_N-GLC_2 | 381 | 383 | PF02516 | 0.520 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.607 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.602 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.467 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.528 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.742 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.691 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.532 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.695 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.441 |
MOD_NEK2_2 | 307 | 312 | PF00069 | 0.393 |
MOD_NEK2_2 | 505 | 510 | PF00069 | 0.592 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.556 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.706 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.692 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.588 |
MOD_PK_1 | 214 | 220 | PF00069 | 0.648 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.632 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.614 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.545 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.659 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.719 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.629 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.730 |
MOD_PKB_1 | 101 | 109 | PF00069 | 0.588 |
MOD_PKB_1 | 352 | 360 | PF00069 | 0.533 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.541 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.441 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.468 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.699 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.587 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.560 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.502 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.500 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.592 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.441 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.742 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.574 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.519 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.715 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.559 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.709 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.756 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.577 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.591 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.745 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.509 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.713 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.571 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.684 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.623 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.612 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.717 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.698 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.577 |
TRG_NLS_Bipartite_1 | 222 | 237 | PF00514 | 0.618 |
TRG_NLS_MonoExtC_3 | 349 | 354 | PF00514 | 0.502 |
TRG_NLS_MonoExtN_4 | 118 | 123 | PF00514 | 0.775 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IIS4 | Leishmania donovani | 63% | 98% |
A4I4J6 | Leishmania infantum | 63% | 98% |
E9ADZ5 | Leishmania major | 63% | 100% |
E9ALT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 97% |