A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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: 35 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 38 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AJJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 39 |
GO:0006793 | phosphorus metabolic process | 3 | 39 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 39 |
GO:0006807 | nitrogen compound metabolic process | 2 | 39 |
GO:0008152 | metabolic process | 1 | 39 |
GO:0009987 | cellular process | 1 | 39 |
GO:0016310 | phosphorylation | 5 | 39 |
GO:0019538 | protein metabolic process | 3 | 39 |
GO:0036211 | protein modification process | 4 | 39 |
GO:0043170 | macromolecule metabolic process | 3 | 39 |
GO:0043412 | macromolecule modification | 4 | 39 |
GO:0044237 | cellular metabolic process | 2 | 39 |
GO:0044238 | primary metabolic process | 2 | 39 |
GO:0071704 | organic substance metabolic process | 2 | 39 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 39 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 39 |
GO:0003824 | catalytic activity | 1 | 39 |
GO:0004672 | protein kinase activity | 3 | 39 |
GO:0005488 | binding | 1 | 39 |
GO:0005524 | ATP binding | 5 | 39 |
GO:0016301 | kinase activity | 4 | 39 |
GO:0016740 | transferase activity | 2 | 39 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 39 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 39 |
GO:0017076 | purine nucleotide binding | 4 | 39 |
GO:0030554 | adenyl nucleotide binding | 5 | 39 |
GO:0032553 | ribonucleotide binding | 3 | 39 |
GO:0032555 | purine ribonucleotide binding | 4 | 39 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 39 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 39 |
GO:0036094 | small molecule binding | 2 | 39 |
GO:0043167 | ion binding | 2 | 39 |
GO:0043168 | anion binding | 3 | 39 |
GO:0097159 | organic cyclic compound binding | 2 | 39 |
GO:0097367 | carbohydrate derivative binding | 2 | 39 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 39 |
GO:1901265 | nucleoside phosphate binding | 3 | 39 |
GO:1901363 | heterocyclic compound binding | 2 | 39 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.307 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.247 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 446 | 452 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.246 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.240 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.379 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.468 |
DEG_SIAH_1 | 73 | 81 | PF03145 | 0.463 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.470 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.240 |
DEG_SPOP_SBC_1 | 276 | 280 | PF00917 | 0.391 |
DOC_ANK_TNKS_1 | 493 | 500 | PF00023 | 0.435 |
DOC_CDC14_PxL_1 | 361 | 369 | PF14671 | 0.299 |
DOC_CKS1_1 | 488 | 493 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 389 | 400 | PF00134 | 0.202 |
DOC_CYCLIN_yCln2_LP_2 | 291 | 297 | PF00134 | 0.166 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.330 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.195 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.740 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.226 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 494 | 501 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 81 | 85 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 434 | 452 | PF00022 | 0.243 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.266 |
LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.659 |
LIG_Clathr_ClatBox_1 | 438 | 442 | PF01394 | 0.286 |
LIG_deltaCOP1_diTrp_1 | 378 | 386 | PF00928 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 6 | 10 | PF00928 | 0.573 |
LIG_eIF4E_1 | 362 | 368 | PF01652 | 0.231 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.526 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.250 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.323 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.686 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.339 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.191 |
LIG_HOMEOBOX | 5 | 8 | PF00046 | 0.470 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 498 | 509 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.461 |
LIG_Rb_pABgroove_1 | 221 | 229 | PF01858 | 0.302 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.314 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.420 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.323 |
LIG_SH2_SRC | 464 | 467 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 128 | 131 | PF00017 | 0.555 |
LIG_SH2_STAT3 | 427 | 430 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.358 |
LIG_SH3_2 | 475 | 480 | PF14604 | 0.428 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.256 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.199 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.555 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.568 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.448 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.351 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.201 |
LIG_WW_1 | 231 | 234 | PF00397 | 0.191 |
MOD_CDK_SPxxK_3 | 487 | 494 | PF00069 | 0.456 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.488 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.319 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.302 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.344 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.235 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.490 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.733 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.702 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.494 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.323 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.404 |
MOD_Cter_Amidation | 254 | 257 | PF01082 | 0.191 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.670 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.541 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.572 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.369 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.368 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.598 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.439 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.566 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.810 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.485 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.218 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.377 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.363 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.284 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.533 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.558 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.406 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.333 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.333 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.243 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.219 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.446 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.239 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.410 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.306 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.201 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.460 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.411 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.521 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.487 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.303 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.417 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.445 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.660 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.278 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.316 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.251 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.338 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.215 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.423 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.556 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.506 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.226 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.319 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.352 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.466 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.529 |
MOD_SUMO_rev_2 | 205 | 210 | PF00179 | 0.285 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.201 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.262 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.177 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.245 |
TRG_NES_CRM1_1 | 331 | 345 | PF08389 | 0.201 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2D3 | Leptomonas seymouri | 51% | 100% |
A0A0N1HTF0 | Leptomonas seymouri | 23% | 85% |
A0A0N1HZW6 | Leptomonas seymouri | 26% | 100% |
A0A0S4IZ14 | Bodo saltans | 23% | 91% |
A0A0S4J757 | Bodo saltans | 26% | 100% |
A0A0S4JIJ6 | Bodo saltans | 26% | 95% |
A0A0S4JKY4 | Bodo saltans | 31% | 68% |
A0A0S4JMY6 | Bodo saltans | 25% | 70% |
A0A0S4JPZ1 | Bodo saltans | 27% | 100% |
A0A1X0NKA1 | Trypanosomatidae | 39% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 25% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 32% | 100% |
A0A3Q8IDY1 | Leishmania donovani | 27% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 29% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 31% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 28% | 100% |
A0A3Q8IPJ5 | Leishmania donovani | 26% | 100% |
A0A3S5H4Z4 | Leishmania donovani | 89% | 100% |
A0A3S7WUE7 | Leishmania donovani | 26% | 97% |
A0A3S7X6T8 | Leishmania donovani | 27% | 100% |
A0A422N701 | Trypanosoma rangeli | 40% | 100% |
A4H3C7 | Leishmania braziliensis | 75% | 100% |
A4HC09 | Leishmania braziliensis | 31% | 67% |
A4HCE6 | Leishmania braziliensis | 30% | 100% |
A4HFA1 | Leishmania braziliensis | 26% | 100% |
A4HHP8 | Leishmania braziliensis | 27% | 100% |
A4HJT5 | Leishmania braziliensis | 28% | 100% |
A4HJW2 | Leishmania braziliensis | 31% | 100% |
A4HLR0 | Leishmania braziliensis | 28% | 100% |
A4HRM6 | Leishmania infantum | 89% | 100% |
A4HW76 | Leishmania infantum | 23% | 67% |
A4HX71 | Leishmania infantum | 26% | 97% |
A4HZW8 | Leishmania infantum | 32% | 100% |
A4I2H8 | Leishmania infantum | 26% | 100% |
A4I435 | Leishmania infantum | 28% | 100% |
A4I4W3 | Leishmania infantum | 27% | 100% |
A4I7A1 | Leishmania infantum | 29% | 100% |
A4I7C4 | Leishmania infantum | 31% | 100% |
A4I960 | Leishmania infantum | 27% | 100% |
C9ZIZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZQL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 84% |
C9ZX04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZX09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9ACA4 | Leishmania major | 89% | 100% |
E9AEB1 | Leishmania major | 26% | 100% |
E9ALH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9ARC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 97% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AWZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 89% |
E9AYN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
P24723 | Homo sapiens | 25% | 79% |
P49101 | Zea mays | 27% | 100% |
P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 25% | 100% |
P62344 | Plasmodium falciparum (isolate 3D7) | 25% | 100% |
Q0VD22 | Bos taurus | 24% | 100% |
Q4Q3Y9 | Leishmania major | 27% | 100% |
Q4Q5T9 | Leishmania major | 31% | 100% |
Q4Q5W2 | Leishmania major | 29% | 100% |
Q4Q7W2 | Leishmania major | 28% | 100% |
Q4Q8T4 | Leishmania major | 26% | 100% |
Q4QBQ2 | Leishmania major | 33% | 100% |
Q4QCK0 | Leishmania major | 28% | 100% |
Q4QEJ2 | Leishmania major | 26% | 97% |
Q5VQQ5 | Oryza sativa subsp. japonica | 27% | 100% |
Q64617 | Rattus norvegicus | 25% | 79% |
Q6Z2M9 | Oryza sativa subsp. japonica | 27% | 100% |
Q7SY24 | Danio rerio | 25% | 80% |
Q924X7 | Mus musculus | 24% | 100% |
Q9NJU9 | Plasmodium falciparum (isolate 3D7) | 23% | 96% |
Q9Y243 | Homo sapiens | 26% | 100% |
Q9Y6E0 | Homo sapiens | 25% | 100% |
V5BHW8 | Trypanosoma cruzi | 25% | 85% |
V5D179 | Trypanosoma cruzi | 26% | 89% |