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: 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: 15 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: A0A3S7WTT7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016310 | phosphorylation | 5 | 16 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004672 | protein kinase activity | 3 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016301 | kinase activity | 4 | 16 |
GO:0016740 | transferase activity | 2 | 16 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.741 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.479 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.315 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.578 |
DEG_SCF_FBW7_1 | 502 | 507 | PF00400 | 0.496 |
DOC_CDC14_PxL_1 | 397 | 405 | PF14671 | 0.539 |
DOC_CYCLIN_RxL_1 | 251 | 260 | PF00134 | 0.333 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.306 |
DOC_MAPK_DCC_7 | 396 | 405 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.315 |
DOC_MAPK_HePTP_8 | 393 | 405 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 396 | 405 | PF00069 | 0.633 |
DOC_PP1_RVXF_1 | 224 | 231 | PF00149 | 0.295 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.285 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.677 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.260 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.244 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.334 |
LIG_Actin_WH2_2 | 585 | 600 | PF00022 | 0.598 |
LIG_AP2alpha_2 | 273 | 275 | PF02296 | 0.260 |
LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.265 |
LIG_APCC_ABBAyCdc20_2 | 138 | 144 | PF00400 | 0.393 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.666 |
LIG_deltaCOP1_diTrp_1 | 243 | 252 | PF00928 | 0.260 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.409 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.674 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.294 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.542 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.494 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.690 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.412 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.313 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.250 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.260 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.393 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.315 |
LIG_LIR_Apic_2 | 273 | 278 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 507 | 512 | PF02991 | 0.580 |
LIG_PCNA_yPIPBox_3 | 284 | 298 | PF02747 | 0.503 |
LIG_Rb_LxCxE_1 | 547 | 564 | PF01857 | 0.457 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.276 |
LIG_SH2_CRK | 513 | 517 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.298 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.524 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 208 | 214 | PF11976 | 0.334 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.496 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.614 |
LIG_WW_1 | 510 | 513 | PF00397 | 0.564 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.385 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.371 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.567 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.260 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.477 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.572 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.393 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.633 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.414 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.399 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.595 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.593 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.544 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.682 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.529 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.781 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.536 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.519 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.593 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.291 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.260 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.388 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.499 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.605 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.626 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.556 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.647 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.574 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.602 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.498 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.601 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.567 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.487 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.260 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.260 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.274 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.685 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.516 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.447 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.576 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.476 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.424 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.548 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.479 |
MOD_PK_1 | 322 | 328 | PF00069 | 0.568 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.260 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.500 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.371 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.285 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.260 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.587 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.553 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.262 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.689 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.608 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.577 |
MOD_Plk_2-3 | 101 | 107 | PF00069 | 0.276 |
MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.250 |
MOD_Plk_2-3 | 406 | 412 | PF00069 | 0.667 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.410 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.273 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.286 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.554 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.538 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.542 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.461 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.371 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.260 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.645 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.661 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.464 |
MOD_SUMO_rev_2 | 14 | 20 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 162 | 172 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 579 | 586 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_1 | 534 | 539 | PF01217 | 0.610 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.671 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.578 |
TRG_NES_CRM1_1 | 44 | 58 | PF08389 | 0.260 |
TRG_NES_CRM1_1 | 60 | 74 | PF08389 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.238 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW4 | Leptomonas seymouri | 58% | 100% |
A0A0S4IHW4 | Bodo saltans | 45% | 100% |
A0A3R7K109 | Trypanosoma rangeli | 49% | 100% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4H8F5 | Leishmania braziliensis | 80% | 100% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4HWS9 | Leishmania infantum | 100% | 100% |
C9ZW46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AQI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QEZ0 | Leishmania major | 91% | 100% |
Q4QJJ0 | Leishmania major | 27% | 100% |
V5B141 | Trypanosoma cruzi | 49% | 100% |