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 |
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: A4I5C6
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 | 126 | 130 | PF00656 | 0.741 |
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.726 |
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.762 |
CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.794 |
CLV_PCSK_FUR_1 | 48 | 52 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.791 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 569 | 577 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 633 | 641 | PF00400 | 0.378 |
DEG_MDM2_SWIB_1 | 399 | 406 | PF02201 | 0.447 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.493 |
DOC_CYCLIN_RxL_1 | 212 | 222 | PF00134 | 0.646 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 368 | 377 | PF00134 | 0.437 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 568 | 575 | PF00149 | 0.417 |
DOC_PP2B_LxvP_1 | 590 | 593 | PF13499 | 0.584 |
DOC_PP4_FxxP_1 | 17 | 20 | PF00568 | 0.715 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.491 |
DOC_USP7_MATH_2 | 186 | 192 | PF00917 | 0.690 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 489 | 497 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 605 | 611 | PF00244 | 0.441 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.739 |
LIG_deltaCOP1_diTrp_1 | 240 | 248 | PF00928 | 0.524 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.496 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.469 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.492 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.725 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.419 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.654 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.205 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.497 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.715 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.270 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.549 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.763 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.793 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.623 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.546 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.359 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.606 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.760 |
LIG_LIR_Apic_2 | 15 | 20 | PF02991 | 0.679 |
LIG_LIR_Apic_2 | 251 | 257 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 262 | 272 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 402 | 411 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 402 | 406 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 642 | 646 | PF02991 | 0.577 |
LIG_Pex14_2 | 399 | 403 | PF04695 | 0.435 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.450 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 419 | 422 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 371 | 375 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 261 | 264 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.438 |
LIG_SH3_2 | 22 | 27 | PF14604 | 0.745 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.783 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.502 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.524 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.751 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.423 |
LIG_SH3_5 | 257 | 261 | PF00018 | 0.524 |
LIG_SUMO_SIM_par_1 | 242 | 247 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 355 | 363 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 429 | 435 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 559 | 564 | PF11976 | 0.458 |
LIG_SxIP_EBH_1 | 489 | 503 | PF03271 | 0.492 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.727 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.524 |
LIG_TYR_ITIM | 420 | 425 | PF00017 | 0.422 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.698 |
MOD_CDK_SPxK_1 | 18 | 24 | PF00069 | 0.696 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.798 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.546 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.316 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.657 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.434 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.510 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.422 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.791 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.533 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.390 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.724 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.539 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.607 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.580 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.695 |
MOD_Cter_Amidation | 323 | 326 | PF01082 | 0.640 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.749 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.802 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.716 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.572 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.397 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.750 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.340 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.381 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.410 |
MOD_GlcNHglycan | 435 | 439 | PF01048 | 0.636 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.537 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.498 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.495 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.531 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.709 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.676 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.654 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.649 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.739 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.474 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.592 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.519 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.490 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.655 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.427 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.509 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.355 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.728 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.697 |
MOD_N-GLC_1 | 611 | 616 | PF02516 | 0.506 |
MOD_N-GLC_2 | 160 | 162 | PF02516 | 0.604 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.433 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.415 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.524 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.503 |
MOD_NEK2_2 | 12 | 17 | PF00069 | 0.606 |
MOD_NEK2_2 | 278 | 283 | PF00069 | 0.444 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.524 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.541 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.648 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.512 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.524 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.754 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.645 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.544 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.500 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.456 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.443 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.755 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.713 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.524 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.433 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.665 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.632 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.387 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.406 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.604 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.403 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.387 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.806 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.707 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.430 |
MOD_SUMO_rev_2 | 222 | 230 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 53 | 62 | PF00179 | 0.735 |
TRG_DiLeu_BaLyEn_6 | 544 | 549 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 632 | 637 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 532 | 534 | PF00400 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 215 | 220 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W9 | Leptomonas seymouri | 59% | 97% |
A0A3S7X390 | Leishmania donovani | 100% | 100% |
A0A3S7X6T4 | Leishmania donovani | 23% | 100% |
A4HI50 | Leishmania braziliensis | 76% | 100% |
A4HLQ3 | Leishmania braziliensis | 23% | 100% |
A4I953 | Leishmania infantum | 23% | 100% |
E9B0M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B428 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
O22607 | Arabidopsis thaliana | 22% | 100% |
P0CS36 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 31% | 100% |
P0CS37 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 31% | 100% |
Q4Q3Z6 | Leishmania major | 22% | 100% |
Q4Q7K8 | Leishmania major | 92% | 100% |
Q6C7Q4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 100% |