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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: Q4QAM7
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
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:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
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:0051252 | regulation of RNA metabolic process | 5 | 2 |
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:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 118 | 126 | PF00400 | 0.614 |
DEG_APCC_DBOX_1 | 451 | 459 | PF00400 | 0.536 |
DEG_COP1_1 | 291 | 301 | PF00400 | 0.699 |
DEG_ODPH_VHL_1 | 447 | 458 | PF01847 | 0.530 |
DEG_SPOP_SBC_1 | 581 | 585 | PF00917 | 0.419 |
DOC_CDC14_PxL_1 | 565 | 573 | PF14671 | 0.536 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.574 |
DOC_MAPK_DCC_7 | 563 | 573 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 405 | 411 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 393 | 400 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.555 |
DOC_MAPK_NFAT4_5 | 393 | 401 | PF00069 | 0.471 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 90 | 93 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 227 | 230 | PF00568 | 0.651 |
DOC_PP4_FxxP_1 | 473 | 476 | PF00568 | 0.510 |
DOC_PP4_FxxP_1 | 566 | 569 | PF00568 | 0.536 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.664 |
DOC_USP7_UBL2_3 | 530 | 534 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 35 | 42 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 48 | 52 | PF00244 | 0.501 |
LIG_APCC_ABBA_1 | 123 | 128 | PF00400 | 0.621 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.452 |
LIG_BIR_III_2 | 543 | 547 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.501 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_2 | 323 | 329 | PF00533 | 0.487 |
LIG_CaM_IQ_9 | 105 | 121 | PF13499 | 0.557 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.644 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.329 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.522 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.526 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.531 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.544 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.737 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.587 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.535 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.610 |
LIG_LIR_Apic_2 | 472 | 476 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.444 |
LIG_PDZ_Class_2 | 589 | 594 | PF00595 | 0.496 |
LIG_Pex14_2 | 420 | 424 | PF04695 | 0.536 |
LIG_PTB_Apo_2 | 218 | 225 | PF02174 | 0.604 |
LIG_PTB_Phospho_1 | 218 | 224 | PF10480 | 0.604 |
LIG_SH2_PTP2 | 7 | 10 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.582 |
LIG_SH3_1 | 7 | 13 | PF00018 | 0.460 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.771 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.754 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.595 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.721 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.504 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.508 |
LIG_SH3_CIN85_PxpxPR_1 | 233 | 238 | PF14604 | 0.653 |
LIG_SUMO_SIM_anti_2 | 101 | 109 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 397 | 402 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.458 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.510 |
LIG_TRFH_1 | 165 | 169 | PF08558 | 0.566 |
LIG_TYR_ITIM | 481 | 486 | PF00017 | 0.471 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.536 |
LIG_WW_3 | 308 | 312 | PF00397 | 0.654 |
MOD_CDK_SPxxK_3 | 229 | 236 | PF00069 | 0.576 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.532 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.729 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.639 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.554 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.588 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.563 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.455 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.496 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.556 |
MOD_Cter_Amidation | 133 | 136 | PF01082 | 0.745 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.482 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.506 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.757 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.759 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.499 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.297 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.385 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.310 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.561 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.703 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.372 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.533 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.515 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.516 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.523 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.528 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.519 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.708 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.296 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.515 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.716 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.562 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.413 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.532 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.513 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.471 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.589 |
MOD_NEK2_2 | 588 | 593 | PF00069 | 0.510 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.541 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.554 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.533 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.589 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.496 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.586 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.472 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.507 |
MOD_Plk_1 | 588 | 594 | PF00069 | 0.535 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.539 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.509 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.534 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.476 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.587 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.588 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.573 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.748 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.623 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.595 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 60 | 63 | PF00400 | 0.525 |
TRG_NES_CRM1_1 | 158 | 170 | PF08389 | 0.513 |
TRG_NLS_Bipartite_1 | 520 | 537 | PF00514 | 0.522 |
TRG_NLS_MonoExtN_4 | 530 | 537 | PF00514 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 500 | 504 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 545 | 549 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 563 | 567 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X3 | Leptomonas seymouri | 58% | 100% |
A0A3S7WYE0 | Leishmania donovani | 92% | 100% |
A0A422MP50 | Trypanosoma rangeli | 28% | 100% |
A4HDG2 | Leishmania braziliensis | 77% | 100% |
A4I0U3 | Leishmania infantum | 93% | 100% |
C9ZVE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AWU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |