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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H574
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003713 | transcription coactivator activity | 3 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 126 | 130 | PF00082 | 0.694 |
CLV_PCSK_FUR_1 | 233 | 237 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.409 |
DEG_APCC_KENBOX_2 | 302 | 306 | PF00400 | 0.720 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.456 |
DOC_CKS1_1 | 96 | 101 | PF01111 | 0.578 |
DOC_CYCLIN_yCln2_LP_2 | 598 | 604 | PF00134 | 0.346 |
DOC_MAPK_DCC_7 | 596 | 604 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 125 | 133 | PF00069 | 0.646 |
DOC_MAPK_gen_1 | 427 | 435 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 371 | 380 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 427 | 434 | PF00069 | 0.413 |
DOC_MAPK_NFAT4_5 | 427 | 435 | PF00069 | 0.418 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.281 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.373 |
DOC_SPAK_OSR1_1 | 474 | 478 | PF12202 | 0.438 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.366 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.595 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 371 | 376 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 466 | 472 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 616 | 625 | PF00244 | 0.389 |
LIG_BIR_III_2 | 310 | 314 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 471 | 475 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.452 |
LIG_Clathr_ClatBox_1 | 610 | 614 | PF01394 | 0.374 |
LIG_EH1_1 | 474 | 482 | PF00400 | 0.439 |
LIG_eIF4E_1 | 553 | 559 | PF01652 | 0.266 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.706 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.429 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.397 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.611 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.266 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.266 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.385 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.353 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.602 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.616 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.210 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.479 |
LIG_LIR_Apic_2 | 252 | 257 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 536 | 545 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 585 | 595 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.340 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.266 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 573 | 577 | PF00017 | 0.276 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.266 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.596 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 450 | 454 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.266 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.583 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.561 |
LIG_SH3_4 | 8 | 15 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 431 | 436 | PF11976 | 0.666 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.414 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.584 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.704 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.266 |
MOD_CDK_SPxxK_3 | 347 | 354 | PF00069 | 0.596 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.658 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.529 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.382 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.586 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.702 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.717 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.480 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.210 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.357 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.702 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.608 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.313 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.465 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.623 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.530 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.527 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.210 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.316 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.545 |
MOD_Cter_Amidation | 361 | 364 | PF01082 | 0.650 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.459 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.550 |
MOD_GlcNHglycan | 241 | 246 | PF01048 | 0.564 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.544 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.566 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.695 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.647 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.616 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.617 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.542 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.693 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.496 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.694 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.392 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.309 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.570 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.655 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.715 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.421 |
MOD_N-GLC_1 | 604 | 609 | PF02516 | 0.298 |
MOD_N-GLC_2 | 18 | 20 | PF02516 | 0.406 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.476 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.633 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.448 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.494 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.298 |
MOD_NEK2_2 | 155 | 160 | PF00069 | 0.482 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.607 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.766 |
MOD_PK_1 | 371 | 377 | PF00069 | 0.495 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.608 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.625 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.655 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.519 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.451 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.625 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.489 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.655 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.734 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.582 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.605 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.625 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.606 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.568 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.505 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.589 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.171 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.468 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.380 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.459 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.481 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.711 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.350 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.507 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 589 | 598 | PF00179 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.281 |
TRG_NLS_MonoExtC_3 | 124 | 129 | PF00514 | 0.699 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 623 | 627 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGL1 | Leptomonas seymouri | 69% | 100% |
A0A0S4IUQ4 | Bodo saltans | 38% | 98% |
A0A1X0NNW7 | Trypanosomatidae | 43% | 98% |
A0A3S5H626 | Leishmania donovani | 79% | 100% |
A0A3S5IQP6 | Trypanosoma rangeli | 47% | 100% |
A4HTF7 | Leishmania infantum | 79% | 100% |
C9ZPN3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AM85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QIG2 | Leishmania major | 77% | 100% |
V5BH64 | Trypanosoma cruzi | 46% | 100% |