A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 23 |
NetGPI | no | yes: 0, no: 23 |
Related structures:
AlphaFold database: A4H7W1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 24 |
GO:0006793 | phosphorus metabolic process | 3 | 24 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 24 |
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0016310 | phosphorylation | 5 | 24 |
GO:0019538 | protein metabolic process | 3 | 24 |
GO:0036211 | protein modification process | 4 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0043412 | macromolecule modification | 4 | 24 |
GO:0044237 | cellular metabolic process | 2 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 24 |
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 | 24 |
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004672 | protein kinase activity | 3 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0016301 | kinase activity | 4 | 24 |
GO:0016740 | transferase activity | 2 | 24 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 24 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 24 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.540 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.239 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.448 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.209 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.415 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.413 |
DEG_SCF_FBW7_1 | 520 | 525 | PF00400 | 0.482 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.786 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.321 |
DOC_CKS1_1 | 349 | 354 | PF01111 | 0.528 |
DOC_CKS1_1 | 416 | 421 | PF01111 | 0.523 |
DOC_CKS1_1 | 507 | 512 | PF01111 | 0.466 |
DOC_CKS1_1 | 519 | 524 | PF01111 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 201 | 207 | PF00134 | 0.230 |
DOC_CYCLIN_yCln2_LP_2 | 520 | 526 | PF00134 | 0.532 |
DOC_MAPK_DCC_7 | 379 | 389 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 129 | 138 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 248 | 257 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 73 | 80 | PF00069 | 0.236 |
DOC_MAPK_gen_1 | 95 | 102 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 250 | 259 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.355 |
DOC_MAPK_RevD_3 | 112 | 125 | PF00069 | 0.316 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.317 |
DOC_PP2B_LxvP_1 | 342 | 345 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.498 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.468 |
DOC_PP4_FxxP_1 | 416 | 419 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.347 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.230 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 431 | 436 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 45 | 50 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 491 | 501 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.454 |
LIG_APCC_ABBAyCdc20_2 | 124 | 130 | PF00400 | 0.373 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.740 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.230 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.368 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.302 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.485 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.353 |
LIG_LIR_Apic_2 | 413 | 419 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.535 |
LIG_LIR_Apic_2 | 499 | 505 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.312 |
LIG_MAD2 | 216 | 224 | PF02301 | 0.316 |
LIG_MAD2 | 53 | 61 | PF02301 | 0.230 |
LIG_MYND_1 | 501 | 505 | PF01753 | 0.477 |
LIG_MYND_1 | 522 | 526 | PF01753 | 0.516 |
LIG_PDZ_Class_3 | 544 | 549 | PF00595 | 0.435 |
LIG_PTB_Apo_2 | 501 | 508 | PF02174 | 0.487 |
LIG_PTB_Phospho_1 | 501 | 507 | PF10480 | 0.428 |
LIG_RPA_C_Fungi | 531 | 543 | PF08784 | 0.400 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.260 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.465 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.693 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.345 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.536 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.478 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.519 |
LIG_SH2_GRB2like | 381 | 384 | PF00017 | 0.495 |
LIG_SH2_GRB2like | 502 | 505 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.536 |
LIG_SH2_SRC | 502 | 505 | PF00017 | 0.470 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.230 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 120 | 123 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 388 | 391 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 465 | 468 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.320 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.373 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.230 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.514 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.470 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.511 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.524 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.523 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.268 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.282 |
LIG_TRFH_1 | 170 | 174 | PF08558 | 0.313 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.277 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.230 |
LIG_WRC_WIRS_1 | 67 | 72 | PF05994 | 0.335 |
MOD_CDK_SPK_2 | 297 | 302 | PF00069 | 0.399 |
MOD_CDK_SPK_2 | 506 | 511 | PF00069 | 0.460 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.540 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.516 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.717 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.690 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.509 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.574 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.516 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.427 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.334 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.311 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.677 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.650 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.697 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.541 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.641 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.455 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.505 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.230 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.302 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.340 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.292 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.282 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.622 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.636 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.610 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.499 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.475 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.475 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.512 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.487 |
MOD_LATS_1 | 396 | 402 | PF00433 | 0.528 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.565 |
MOD_N-GLC_2 | 77 | 79 | PF02516 | 0.230 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.703 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.456 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.230 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.271 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.487 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.517 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.234 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.439 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.260 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.358 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.481 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.593 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.308 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.329 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.484 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.597 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.471 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.542 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.486 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.532 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.470 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.484 |
MOD_SUMO_for_1 | 249 | 252 | PF00179 | 0.261 |
MOD_SUMO_rev_2 | 206 | 213 | PF00179 | 0.175 |
MOD_SUMO_rev_2 | 525 | 533 | PF00179 | 0.417 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 329 | 332 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.464 |
TRG_NES_CRM1_1 | 106 | 119 | PF08389 | 0.276 |
TRG_NES_CRM1_1 | 209 | 223 | PF08389 | 0.230 |
TRG_NES_CRM1_1 | 232 | 244 | PF08389 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.244 |
TRG_Pf-PMV_PEXEL_1 | 332 | 336 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A0 | Leptomonas seymouri | 28% | 84% |
A0A0S4IQ75 | Bodo saltans | 31% | 100% |
A0A0S4JIJ6 | Bodo saltans | 29% | 97% |
A0A3Q8IB74 | Leishmania donovani | 24% | 100% |
A0A3Q8IC87 | Leishmania donovani | 30% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 36% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 30% | 100% |
A0A3Q8IIH5 | Leishmania donovani | 77% | 99% |
A0A3Q8INQ4 | Leishmania donovani | 27% | 100% |
A0A3S5H789 | Leishmania donovani | 25% | 100% |
A0A3S7X2W3 | Leishmania donovani | 27% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 28% | 100% |
A4H9X5 | Leishmania braziliensis | 23% | 100% |
A4HAS1 | Leishmania braziliensis | 29% | 100% |
A4HED7 | Leishmania braziliensis | 27% | 100% |
A4HFC9 | Leishmania braziliensis | 25% | 83% |
A4HH03 | Leishmania braziliensis | 31% | 100% |
A4HHN1 | Leishmania braziliensis | 27% | 100% |
A4HJT5 | Leishmania braziliensis | 36% | 100% |
A4HW88 | Leishmania infantum | 77% | 99% |
A4HYX6 | Leishmania infantum | 25% | 100% |
A4HZV1 | Leishmania infantum | 30% | 100% |
A4I1T4 | Leishmania infantum | 27% | 100% |
A4I435 | Leishmania infantum | 30% | 100% |
A4I4U6 | Leishmania infantum | 27% | 100% |
A4I7A1 | Leishmania infantum | 36% | 100% |
A4I9Y5 | Leishmania infantum | 28% | 100% |
E9AGS0 | Leishmania infantum | 24% | 100% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9APY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 99% |
E9ARW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AUS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q2Z2 | Leishmania major | 28% | 100% |
Q4Q3K6 | Leishmania major | 24% | 100% |
Q4Q5W2 | Leishmania major | 36% | 100% |
Q4Q7W2 | Leishmania major | 30% | 100% |
Q4Q9K2 | Leishmania major | 27% | 100% |
Q4QBR6 | Leishmania major | 30% | 100% |
Q4QCR3 | Leishmania major | 24% | 100% |
Q4QDK3 | Leishmania major | 24% | 100% |
Q4QFJ2 | Leishmania major | 77% | 100% |
Q7KZI7 | Homo sapiens | 28% | 70% |
Q9Y077 | Leishmania major | 27% | 100% |
V5BAZ8 | Trypanosoma cruzi | 26% | 100% |