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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WTG9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.641 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.302 |
CLV_PCSK_PC7_1 | 646 | 652 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.302 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.703 |
DOC_CYCLIN_RxL_1 | 83 | 96 | PF00134 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.396 |
DOC_MAPK_gen_1 | 194 | 203 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.321 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.291 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.346 |
DOC_PP4_FxxP_1 | 624 | 627 | PF00568 | 0.735 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 151 | 161 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 646 | 654 | PF00244 | 0.666 |
LIG_AP2alpha_1 | 500 | 504 | PF02296 | 0.628 |
LIG_AP2alpha_1 | 654 | 658 | PF02296 | 0.643 |
LIG_AP2alpha_2 | 256 | 258 | PF02296 | 0.427 |
LIG_AP2alpha_2 | 652 | 654 | PF02296 | 0.596 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.795 |
LIG_deltaCOP1_diTrp_1 | 295 | 301 | PF00928 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 357 | 362 | PF00928 | 0.537 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.318 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.328 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.759 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.418 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.427 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.411 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.427 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.579 |
LIG_Integrin_isoDGR_2 | 417 | 419 | PF01839 | 0.668 |
LIG_LIR_Apic_2 | 382 | 386 | PF02991 | 0.744 |
LIG_LIR_Apic_2 | 622 | 627 | PF02991 | 0.740 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 498 | 507 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 652 | 658 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 652 | 657 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.335 |
LIG_LYPXL_yS_3 | 555 | 558 | PF13949 | 0.683 |
LIG_MAD2 | 368 | 376 | PF02301 | 0.633 |
LIG_MYND_1 | 549 | 553 | PF01753 | 0.628 |
LIG_Pex14_1 | 297 | 301 | PF04695 | 0.427 |
LIG_Pex14_2 | 500 | 504 | PF04695 | 0.628 |
LIG_Pex14_2 | 654 | 658 | PF04695 | 0.599 |
LIG_PTAP_UEV_1 | 522 | 527 | PF05743 | 0.715 |
LIG_PTB_Apo_2 | 243 | 250 | PF02174 | 0.411 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.358 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.736 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.719 |
LIG_SH2_NCK_1 | 608 | 612 | PF00017 | 0.740 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.321 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.308 |
LIG_SH2_SRC | 608 | 611 | PF00017 | 0.740 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.375 |
LIG_SH2_STAT3 | 585 | 588 | PF00017 | 0.755 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.330 |
LIG_SH3_1 | 608 | 614 | PF00018 | 0.670 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.427 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.427 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.388 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.622 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.748 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.566 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.701 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.691 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.704 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.354 |
LIG_SUMO_SIM_anti_2 | 34 | 41 | PF11976 | 0.390 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.427 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.671 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.730 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.508 |
LIG_WW_1 | 54 | 57 | PF00397 | 0.665 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.332 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.388 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.415 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.616 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.479 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.360 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.427 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.456 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.552 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.676 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.512 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.424 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.346 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.700 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.576 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.769 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.700 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.803 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.671 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.642 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.667 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.651 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.414 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.430 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.526 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.598 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.696 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.725 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.712 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.420 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.302 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.323 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.356 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.566 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.677 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.712 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.719 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.472 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.350 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.273 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.277 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.685 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.806 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.464 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.392 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.433 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.777 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.412 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.632 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.356 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.721 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.670 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 111 | 121 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 360 | 370 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 35 | 40 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.719 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.354 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.720 |
TRG_NLS_MonoExtC_3 | 259 | 265 | PF00514 | 0.427 |
TRG_NLS_MonoExtN_4 | 257 | 264 | PF00514 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.793 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7R8 | Leptomonas seymouri | 63% | 94% |
A0A1X0NUC1 | Trypanosomatidae | 44% | 87% |
A0A422NRC0 | Trypanosoma rangeli | 41% | 96% |
A4H848 | Leishmania braziliensis | 67% | 99% |
A4HWH3 | Leishmania infantum | 100% | 100% |
C9ZXX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AQ75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4QFA8 | Leishmania major | 90% | 100% |
V5BK24 | Trypanosoma cruzi | 41% | 96% |