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 | 2 |
GO:0016592 | mediator complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QGT0
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:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0051301 | cell division | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 2 |
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:0097472 | cyclin-dependent protein kinase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 481 | 485 | PF00656 | 0.791 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.814 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.318 |
DEG_APCC_DBOX_1 | 138 | 146 | PF00400 | 0.368 |
DEG_SCF_FBW7_1 | 351 | 356 | PF00400 | 0.318 |
DEG_SCF_FBW7_2 | 425 | 431 | PF00400 | 0.425 |
DEG_SCF_TRCP1_1 | 475 | 481 | PF00400 | 0.557 |
DOC_CKS1_1 | 355 | 360 | PF01111 | 0.318 |
DOC_CKS1_1 | 425 | 430 | PF01111 | 0.439 |
DOC_CYCLIN_RxL_1 | 551 | 560 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 168 | 174 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 313 | 319 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 160 | 169 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 231 | 237 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.351 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.583 |
DOC_PP2B_PxIxI_1 | 133 | 139 | PF00149 | 0.403 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.537 |
DOC_PP4_MxPP_1 | 317 | 320 | PF00568 | 0.513 |
DOC_SPAK_OSR1_1 | 8 | 12 | PF12202 | 0.318 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 231 | 236 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 520 | 524 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 564 | 571 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 41 | 57 | PF00022 | 0.367 |
LIG_APCC_ABBA_1 | 235 | 240 | PF00400 | 0.550 |
LIG_CtBP_PxDLS_1 | 92 | 96 | PF00389 | 0.318 |
LIG_deltaCOP1_diTrp_1 | 376 | 385 | PF00928 | 0.297 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.318 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.318 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.320 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.563 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.557 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.493 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.403 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.318 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.407 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.318 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 410 | 418 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 539 | 550 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 7 | 15 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 89 | 93 | PF02991 | 0.333 |
LIG_MYND_1 | 319 | 323 | PF01753 | 0.505 |
LIG_MYND_1 | 574 | 578 | PF01753 | 0.539 |
LIG_NRBOX | 552 | 558 | PF00104 | 0.390 |
LIG_Pex14_2 | 98 | 102 | PF04695 | 0.318 |
LIG_PTB_Apo_2 | 97 | 104 | PF02174 | 0.318 |
LIG_PTB_Phospho_1 | 97 | 103 | PF10480 | 0.318 |
LIG_REV1ctd_RIR_1 | 227 | 236 | PF16727 | 0.586 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 90 | 93 | PF00017 | 0.318 |
LIG_SH2_SRC | 542 | 545 | PF00017 | 0.492 |
LIG_SH2_SRC | 559 | 562 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.318 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.574 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.680 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.597 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.634 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.318 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.419 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.707 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.403 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.437 |
LIG_TRAF2_2 | 273 | 278 | PF00917 | 0.579 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.318 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.606 |
LIG_WRC_WIRS_1 | 399 | 404 | PF05994 | 0.475 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.427 |
LIG_WW_3 | 523 | 527 | PF00397 | 0.674 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.351 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.643 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.332 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.596 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.340 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.452 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.416 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.318 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.403 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.238 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.318 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.491 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.511 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.445 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.612 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.712 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.679 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.645 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.362 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.235 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.423 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.303 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.634 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.583 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.340 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.654 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.533 |
MOD_N-GLC_2 | 286 | 288 | PF02516 | 0.649 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.403 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.382 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.475 |
MOD_PK_1 | 231 | 237 | PF00069 | 0.476 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.476 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.557 |
MOD_PKA_1 | 563 | 569 | PF00069 | 0.450 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.512 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.607 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.557 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.637 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.681 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.416 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.318 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.318 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.318 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.577 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.602 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.345 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.438 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.518 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.403 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.318 |
MOD_SUMO_rev_2 | 121 | 126 | PF00179 | 0.270 |
MOD_SUMO_rev_2 | 278 | 284 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 318 | 327 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 475 | 481 | PF00179 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4P5 | Leptomonas seymouri | 54% | 92% |
A0A3Q8ICJ0 | Leishmania donovani | 91% | 100% |
A4H6S9 | Leishmania braziliensis | 77% | 100% |
A4HV57 | Leishmania infantum | 91% | 100% |
E9ANU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |