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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B0K5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 598 | 606 | PF00400 | 0.428 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.784 |
DOC_CDC14_PxL_1 | 369 | 377 | PF14671 | 0.393 |
DOC_MAPK_gen_1 | 176 | 184 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 277 | 286 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 480 | 487 | PF00149 | 0.394 |
DOC_PP1_RVXF_1 | 647 | 653 | PF00149 | 0.297 |
DOC_PP2B_LxvP_1 | 610 | 613 | PF13499 | 0.544 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 169 | 173 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 388 | 395 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 563 | 567 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 599 | 608 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 618 | 626 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 627 | 631 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 578 | 593 | PF00022 | 0.584 |
LIG_BRCT_BRCA1_1 | 552 | 556 | PF00533 | 0.544 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.554 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.531 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.551 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.453 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.517 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.509 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.558 |
LIG_IRF3_LxIS_1 | 559 | 565 | PF10401 | 0.442 |
LIG_LIR_Apic_2 | 136 | 140 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 216 | 220 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.446 |
LIG_PCNA_PIPBox_1 | 303 | 312 | PF02747 | 0.559 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.665 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.764 |
LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.817 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.771 |
LIG_SH2_NCK_1 | 455 | 459 | PF00017 | 0.552 |
LIG_SH2_SRC | 455 | 458 | PF00017 | 0.549 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.794 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 157 | 160 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 57 | 60 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.753 |
LIG_SH3_2 | 519 | 524 | PF14604 | 0.627 |
LIG_SH3_2 | 613 | 618 | PF14604 | 0.414 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.555 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.489 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.562 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.420 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 206 | 211 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 283 | 289 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 364 | 370 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 505 | 511 | PF11976 | 0.484 |
LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.550 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.674 |
LIG_UBA3_1 | 165 | 173 | PF00899 | 0.456 |
LIG_UBA3_1 | 433 | 439 | PF00899 | 0.501 |
LIG_UBA3_1 | 492 | 500 | PF00899 | 0.540 |
LIG_WRC_WIRS_1 | 478 | 483 | PF05994 | 0.574 |
LIG_WW_3 | 50 | 54 | PF00397 | 0.748 |
LIG_WW_3 | 518 | 522 | PF00397 | 0.546 |
MOD_CDC14_SPxK_1 | 646 | 649 | PF00782 | 0.322 |
MOD_CDK_SPxK_1 | 643 | 649 | PF00069 | 0.531 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.550 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.542 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.547 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.485 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.496 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.516 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.577 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.469 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.539 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.768 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.274 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.441 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.471 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.373 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.381 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.571 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.579 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.501 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.479 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.579 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.462 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.554 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.513 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.533 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.514 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.465 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.528 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.466 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.577 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.587 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.485 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.542 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.344 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.543 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.477 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.543 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.547 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.546 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.336 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.643 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.655 |
MOD_PKB_1 | 72 | 80 | PF00069 | 0.756 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.445 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.563 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.647 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.518 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.474 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.417 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.433 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.441 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.429 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.596 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.587 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_1 | 364 | 369 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_4 | 297 | 303 | PF01217 | 0.505 |
TRG_DiLeu_LyEn_5 | 187 | 192 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.668 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.764 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.394 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I169 | Leptomonas seymouri | 44% | 100% |
A0A0S4JB89 | Bodo saltans | 25% | 91% |
A0A1X0P251 | Trypanosomatidae | 38% | 100% |
A0A3S7X349 | Leishmania donovani | 91% | 100% |
A0A422P4U2 | Trypanosoma rangeli | 39% | 100% |
A4HI33 | Leishmania braziliensis | 79% | 100% |
A4I5A9 | Leishmania infantum | 91% | 100% |
C9ZQP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 91% |
Q4Q7M7 | Leishmania major | 89% | 97% |