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 | 1 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8ICJ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0051301 | cell division | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 562 | 564 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.782 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.355 |
DEG_SCF_FBW7_1 | 350 | 355 | PF00400 | 0.335 |
DEG_SCF_FBW7_2 | 424 | 430 | PF00400 | 0.388 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.335 |
DOC_CKS1_1 | 424 | 429 | PF01111 | 0.404 |
DOC_CYCLIN_RxL_1 | 550 | 559 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 168 | 174 | PF00134 | 0.470 |
DOC_MAPK_gen_1 | 160 | 169 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.453 |
DOC_PP2B_PxIxI_1 | 133 | 139 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.586 |
DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.581 |
DOC_SPAK_OSR1_1 | 8 | 12 | PF12202 | 0.335 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.704 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 369 | 375 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 519 | 523 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 563 | 570 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.335 |
LIG_Actin_WH2_2 | 41 | 57 | PF00022 | 0.384 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.594 |
LIG_APCC_ABBAyCdc20_2 | 155 | 161 | PF00400 | 0.342 |
LIG_CtBP_PxDLS_1 | 92 | 96 | PF00389 | 0.335 |
LIG_deltaCOP1_diTrp_1 | 375 | 384 | PF00928 | 0.313 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.335 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.424 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.335 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.528 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.567 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.453 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.335 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.697 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.422 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.335 |
LIG_LIR_Apic_2 | 309 | 315 | PF02991 | 0.584 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 409 | 417 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 538 | 549 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 7 | 15 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.335 |
LIG_MYND_1 | 318 | 322 | PF01753 | 0.520 |
LIG_MYND_1 | 573 | 577 | PF01753 | 0.584 |
LIG_NRBOX | 551 | 557 | PF00104 | 0.398 |
LIG_Pex14_2 | 98 | 102 | PF04695 | 0.335 |
LIG_PTB_Apo_2 | 97 | 104 | PF02174 | 0.335 |
LIG_PTB_Phospho_1 | 97 | 103 | PF10480 | 0.335 |
LIG_REV1ctd_RIR_1 | 226 | 235 | PF16727 | 0.653 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 90 | 93 | PF00017 | 0.335 |
LIG_SH2_SRC | 541 | 544 | PF00017 | 0.508 |
LIG_SH2_SRC | 558 | 561 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.335 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.577 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.734 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.626 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.661 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.335 |
LIG_SUMO_SIM_anti_2 | 467 | 475 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.453 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.823 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.453 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.422 |
LIG_TRAF2_2 | 207 | 212 | PF00917 | 0.595 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.335 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.637 |
LIG_WRC_WIRS_1 | 398 | 403 | PF05994 | 0.515 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.413 |
LIG_WW_3 | 522 | 526 | PF00397 | 0.697 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.389 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.695 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.335 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.696 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.335 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.410 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.630 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.429 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.335 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.453 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.250 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.335 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.591 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.335 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.335 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.658 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.808 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.706 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.761 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.366 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.437 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.313 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.553 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.643 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.335 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.708 |
MOD_N-GLC_1 | 509 | 514 | PF02516 | 0.688 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.526 |
MOD_N-GLC_2 | 285 | 287 | PF02516 | 0.681 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.601 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.453 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.392 |
MOD_NEK2_2 | 394 | 399 | PF00069 | 0.526 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.676 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.695 |
MOD_PK_1 | 55 | 61 | PF00069 | 0.313 |
MOD_PKA_1 | 562 | 568 | PF00069 | 0.483 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.632 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.577 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.684 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.708 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.429 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.335 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.537 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.581 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.313 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.335 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.335 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.608 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.703 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.335 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.404 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.547 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 277 | 284 | PF00179 | 0.683 |
MOD_SUMO_rev_2 | 303 | 313 | PF00179 | 0.655 |
MOD_SUMO_rev_2 | 474 | 480 | PF00179 | 0.756 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4P5 | Leptomonas seymouri | 55% | 92% |
A4H6S9 | Leishmania braziliensis | 78% | 100% |
A4HV57 | Leishmania infantum | 99% | 100% |
E9ANU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QGT0 | Leishmania major | 91% | 100% |