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:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QFA8
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004713 | protein tyrosine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 657 | 659 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.335 |
CLV_PCSK_PC7_1 | 653 | 659 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.335 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.761 |
DOC_CYCLIN_RxL_1 | 83 | 96 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 194 | 203 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 448 | 456 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.355 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.378 |
DOC_PP4_FxxP_1 | 627 | 630 | PF00568 | 0.743 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.818 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.246 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 653 | 661 | PF00244 | 0.706 |
LIG_AP2alpha_1 | 499 | 503 | PF02296 | 0.654 |
LIG_AP2alpha_1 | 661 | 665 | PF02296 | 0.670 |
LIG_AP2alpha_2 | 256 | 258 | PF02296 | 0.447 |
LIG_AP2alpha_2 | 659 | 661 | PF02296 | 0.603 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.301 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.794 |
LIG_deltaCOP1_diTrp_1 | 295 | 300 | PF00928 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 356 | 361 | PF00928 | 0.580 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.377 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.351 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.293 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.362 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.335 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.769 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.434 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.447 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.434 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.447 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.599 |
LIG_Integrin_isoDGR_2 | 416 | 418 | PF01839 | 0.706 |
LIG_LIR_Apic_2 | 381 | 385 | PF02991 | 0.804 |
LIG_LIR_Apic_2 | 625 | 630 | PF02991 | 0.748 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 497 | 506 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 659 | 665 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 497 | 502 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 659 | 664 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.355 |
LIG_LYPXL_yS_3 | 554 | 557 | PF13949 | 0.723 |
LIG_MAD2 | 367 | 375 | PF02301 | 0.671 |
LIG_MYND_1 | 548 | 552 | PF01753 | 0.666 |
LIG_MYND_1 | 609 | 613 | PF01753 | 0.545 |
LIG_Pex14_1 | 296 | 300 | PF04695 | 0.447 |
LIG_Pex14_2 | 499 | 503 | PF04695 | 0.654 |
LIG_Pex14_2 | 661 | 665 | PF04695 | 0.621 |
LIG_PTAP_UEV_1 | 521 | 526 | PF05743 | 0.771 |
LIG_PTB_Apo_2 | 243 | 250 | PF02174 | 0.434 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.378 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.368 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.788 |
LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.743 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.355 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.342 |
LIG_SH2_SRC | 607 | 610 | PF00017 | 0.783 |
LIG_SH2_STAT3 | 449 | 452 | PF00017 | 0.642 |
LIG_SH2_STAT3 | 584 | 587 | PF00017 | 0.805 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.355 |
LIG_SH3_1 | 607 | 613 | PF00018 | 0.708 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.447 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.659 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.777 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.540 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.775 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.714 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.704 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.378 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.447 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.697 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.542 |
LIG_WW_1 | 54 | 57 | PF00397 | 0.646 |
LIG_WW_2 | 609 | 612 | PF00397 | 0.546 |
MOD_CDK_SPxxK_3 | 306 | 313 | PF00069 | 0.246 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.544 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.365 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.459 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.430 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.668 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.603 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.649 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.485 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.390 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.447 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.468 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.578 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.721 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.391 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.378 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.696 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.643 |
MOD_GlcNHglycan | 480 | 484 | PF01048 | 0.794 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.750 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.815 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.698 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.667 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.698 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.721 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.782 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.672 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.459 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.262 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.437 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.547 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.727 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.743 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.741 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.571 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.782 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.441 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.334 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.335 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.356 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.304 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.563 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.698 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.730 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.734 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.378 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.765 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.724 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.438 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.360 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.710 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.486 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.793 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.324 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.246 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.449 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.659 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.378 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.246 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.768 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.753 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.695 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.757 |
MOD_SUMO_rev_2 | 111 | 121 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 359 | 369 | PF00179 | 0.587 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.740 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.715 |
TRG_NLS_MonoExtC_3 | 259 | 265 | PF00514 | 0.447 |
TRG_NLS_MonoExtN_4 | 257 | 264 | PF00514 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 313 | 317 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 393 | 398 | PF00026 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7R8 | Leptomonas seymouri | 66% | 95% |
A0A1X0NUC1 | Trypanosomatidae | 45% | 88% |
A0A3S7WTG9 | Leishmania donovani | 90% | 100% |
A0A422NRC0 | Trypanosoma rangeli | 41% | 98% |
A4H848 | Leishmania braziliensis | 65% | 99% |
A4HWH3 | Leishmania infantum | 90% | 100% |
C9ZXX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AQ75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5BK24 | Trypanosoma cruzi | 41% | 98% |