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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0005840 | ribosome | 5 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
Related structures:
AlphaFold database: A4HI50
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.566 |
CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.565 |
CLV_PCSK_PC7_1 | 121 | 127 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.389 |
DEG_APCC_DBOX_1 | 588 | 596 | PF00400 | 0.582 |
DEG_MDM2_SWIB_1 | 418 | 425 | PF02201 | 0.408 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.542 |
DOC_ANK_TNKS_1 | 197 | 204 | PF00023 | 0.528 |
DOC_CDC14_PxL_1 | 26 | 34 | PF14671 | 0.534 |
DOC_CYCLIN_RxL_1 | 231 | 241 | PF00134 | 0.633 |
DOC_MAPK_MEF2A_6 | 302 | 310 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 587 | 594 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 609 | 612 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 17 | 20 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.381 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 508 | 516 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 552 | 557 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 624 | 632 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.288 |
LIG_deltaCOP1_diTrp_1 | 259 | 267 | PF00928 | 0.517 |
LIG_EVH1_1 | 17 | 21 | PF00568 | 0.524 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.493 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.493 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.447 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.587 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.415 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.391 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.518 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.558 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.425 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.651 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.490 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.565 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.451 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.536 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 15 | 20 | PF02991 | 0.599 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 421 | 430 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 613 | 622 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.425 |
LIG_Pex14_1 | 559 | 563 | PF04695 | 0.451 |
LIG_Pex14_2 | 418 | 422 | PF04695 | 0.397 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.536 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.421 |
LIG_SH2_CRK | 652 | 656 | PF00017 | 0.525 |
LIG_SH2_GRB2like | 438 | 441 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 280 | 284 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.354 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.615 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.493 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.552 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.481 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.394 |
LIG_SH3_5 | 276 | 280 | PF00018 | 0.493 |
LIG_SUMO_SIM_par_1 | 261 | 266 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 374 | 382 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 577 | 583 | PF11976 | 0.494 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.476 |
LIG_TYR_ITIM | 282 | 287 | PF00017 | 0.493 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.381 |
MOD_CDK_SPxxK_3 | 128 | 135 | PF00069 | 0.583 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.777 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.643 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.586 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.614 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.409 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.461 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.362 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.403 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.708 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.437 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.633 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.515 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.530 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.771 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.550 |
MOD_Cter_Amidation | 342 | 345 | PF01082 | 0.599 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.769 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.581 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.382 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.386 |
MOD_GlcNHglycan | 454 | 458 | PF01048 | 0.566 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.419 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.437 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.553 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.404 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.584 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.664 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.641 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.711 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.476 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.524 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.559 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.483 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.481 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.294 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.626 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.673 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.672 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.519 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.547 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.508 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.399 |
MOD_N-GLC_1 | 509 | 514 | PF02516 | 0.360 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.459 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.394 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.438 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.427 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.483 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.444 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.605 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.694 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.472 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.614 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.499 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.573 |
MOD_PKA_1 | 552 | 558 | PF00069 | 0.315 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.586 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.434 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.605 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.499 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.481 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.407 |
MOD_PKB_1 | 124 | 132 | PF00069 | 0.515 |
MOD_PKB_1 | 219 | 227 | PF00069 | 0.623 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.521 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.519 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.493 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.505 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.412 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.405 |
MOD_Plk_2-3 | 182 | 188 | PF00069 | 0.538 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.462 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.468 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.412 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.673 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.493 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.354 |
MOD_SUMO_rev_2 | 54 | 62 | PF00179 | 0.634 |
MOD_SUMO_rev_2 | 68 | 75 | PF00179 | 0.557 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 234 | 239 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W9 | Leptomonas seymouri | 58% | 100% |
A0A3S7X390 | Leishmania donovani | 76% | 100% |
A4HD80 | Leishmania braziliensis | 23% | 100% |
A4I5C6 | Leishmania infantum | 76% | 100% |
E9AWL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B0M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q7K8 | Leishmania major | 74% | 97% |
Q9SU78 | Arabidopsis thaliana | 23% | 100% |