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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005952 | cAMP-dependent protein kinase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 1 |
GO:1902911 | protein kinase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: Q4Q1J2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 27 |
GO:0006793 | phosphorus metabolic process | 3 | 27 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0009987 | cellular process | 1 | 27 |
GO:0016310 | phosphorylation | 5 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0044237 | cellular metabolic process | 2 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 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 | 27 |
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004672 | protein kinase activity | 3 | 27 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 26 |
GO:0005488 | binding | 1 | 27 |
GO:0005524 | ATP binding | 5 | 27 |
GO:0016301 | kinase activity | 4 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 27 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 27 |
GO:0017076 | purine nucleotide binding | 4 | 27 |
GO:0030554 | adenyl nucleotide binding | 5 | 27 |
GO:0032553 | ribonucleotide binding | 3 | 27 |
GO:0032555 | purine ribonucleotide binding | 4 | 27 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 27 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 27 |
GO:0036094 | small molecule binding | 2 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043168 | anion binding | 3 | 27 |
GO:0097159 | organic cyclic compound binding | 2 | 27 |
GO:0097367 | carbohydrate derivative binding | 2 | 27 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 27 |
GO:1901265 | nucleoside phosphate binding | 3 | 27 |
GO:1901363 | heterocyclic compound binding | 2 | 27 |
GO:0004690 | cyclic nucleotide-dependent protein kinase activity | 5 | 1 |
GO:0004691 | cAMP-dependent protein kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.449 |
CLV_PCSK_FUR_1 | 122 | 126 | PF00082 | 0.405 |
CLV_PCSK_FUR_1 | 214 | 218 | PF00082 | 0.170 |
CLV_PCSK_FUR_1 | 471 | 475 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.598 |
CLV_PCSK_PC7_1 | 120 | 126 | PF00082 | 0.411 |
CLV_PCSK_PC7_1 | 210 | 216 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.274 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.268 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.478 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.448 |
DEG_SCF_FBW7_2 | 51 | 58 | PF00400 | 0.511 |
DOC_CKS1_1 | 52 | 57 | PF01111 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.263 |
DOC_MAPK_MEF2A_6 | 63 | 70 | PF00069 | 0.600 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.265 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.200 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 215 | 223 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 283 | 292 | PF00244 | 0.234 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.459 |
LIG_APCC_ABBA_1 | 53 | 58 | PF00400 | 0.515 |
LIG_Clathr_ClatBox_1 | 198 | 202 | PF01394 | 0.361 |
LIG_Clathr_ClatBox_1 | 363 | 367 | PF01394 | 0.344 |
LIG_eIF4E_1 | 90 | 96 | PF01652 | 0.400 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.342 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.315 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.241 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.247 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.344 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.329 |
LIG_Integrin_RGD_1 | 301 | 303 | PF01839 | 0.200 |
LIG_IRF3_LxIS_1 | 66 | 71 | PF10401 | 0.421 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 227 | 238 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.198 |
LIG_LIR_Gen_1 | 358 | 368 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.361 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.279 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.475 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.403 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.200 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.291 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.326 |
LIG_SH2_GRB2like | 352 | 355 | PF00017 | 0.200 |
LIG_SH2_NCK_1 | 111 | 115 | PF00017 | 0.362 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.192 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.316 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.461 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.451 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.526 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.609 |
LIG_SUMO_SIM_anti_2 | 196 | 202 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 362 | 367 | PF11976 | 0.350 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.441 |
LIG_TRFH_1 | 293 | 297 | PF08558 | 0.283 |
LIG_TYR_ITIM | 317 | 322 | PF00017 | 0.412 |
LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.291 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.505 |
MOD_CDK_SPxxK_3 | 464 | 471 | PF00069 | 0.490 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.478 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.301 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.480 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.397 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.479 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.344 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.373 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.286 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.566 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.752 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.343 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.316 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.433 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.392 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.675 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.412 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.601 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.338 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.293 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.470 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.368 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.630 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.433 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.647 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.288 |
MOD_PK_1 | 2 | 8 | PF00069 | 0.425 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.170 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.218 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.305 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.176 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.258 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.283 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.452 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.170 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.318 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.577 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.425 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.322 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.388 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.471 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.200 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.337 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.315 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.677 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 252 | 255 | PF00179 | 0.311 |
MOD_SUMO_for_1 | 307 | 310 | PF00179 | 0.200 |
MOD_SUMO_rev_2 | 398 | 408 | PF00179 | 0.320 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.242 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 471 | 474 | PF00400 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 375 | 379 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J6A0 | Bodo saltans | 25% | 67% |
A0A0S4JI45 | Bodo saltans | 24% | 73% |
A0A0S4JK24 | Bodo saltans | 30% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 36% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 29% | 82% |
A0A1X0NWR7 | Trypanosomatidae | 26% | 93% |
A0A3Q8IAQ1 | Leishmania donovani | 40% | 100% |
A0A3Q8IB30 | Leishmania donovani | 33% | 100% |
A0A3Q8IC87 | Leishmania donovani | 29% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 39% | 100% |
A0A3S7X9R4 | Leishmania donovani | 27% | 100% |
A0A3S7X9S2 | Leishmania donovani | 27% | 100% |
A0A3S7XAX0 | Leishmania donovani | 93% | 100% |
A0A422P4V9 | Trypanosoma rangeli | 23% | 100% |
A4H7V0 | Leishmania braziliensis | 25% | 67% |
A4H9L8 | Leishmania braziliensis | 32% | 100% |
A4HCD7 | Leishmania braziliensis | 28% | 100% |
A4HCE6 | Leishmania braziliensis | 37% | 100% |
A4HJT5 | Leishmania braziliensis | 39% | 100% |
A4HXY2 | Leishmania infantum | 33% | 100% |
A4HZV1 | Leishmania infantum | 29% | 100% |
A4HZW8 | Leishmania infantum | 40% | 100% |
A4I7A1 | Leishmania infantum | 39% | 100% |
A4IBT4 | Leishmania infantum | 27% | 100% |
A4IBT9 | Leishmania infantum | 27% | 100% |
A4IDK3 | Leishmania infantum | 94% | 100% |
A5GFW1 | Sus scrofa | 25% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A7M4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 69% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 83% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 67% |
E9ARP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AT06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
O59790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P51817 | Homo sapiens | 27% | 100% |
P90980 | Caenorhabditis elegans | 27% | 70% |
P92958 | Arabidopsis thaliana | 28% | 93% |
Q27687 | Leishmania major | 33% | 100% |
Q2TA06 | Bos taurus | 27% | 100% |
Q38997 | Arabidopsis thaliana | 28% | 93% |
Q4Q598 | Leishmania major | 31% | 73% |
Q4Q5W2 | Leishmania major | 39% | 100% |
Q4QBQ2 | Leishmania major | 40% | 100% |
Q4QBR6 | Leishmania major | 28% | 100% |
Q4QFK4 | Leishmania major | 25% | 76% |
Q641K5 | Mus musculus | 26% | 72% |
Q6FV07 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q7XIW5 | Oryza sativa subsp. japonica | 28% | 100% |
Q869W6 | Dictyostelium discoideum | 28% | 100% |
Q8C0Q4 | Mus musculus | 28% | 76% |
Q8NG66 | Homo sapiens | 28% | 74% |
Q8WNU8 | Macaca fascicularis | 27% | 75% |
Q91819 | Xenopus laevis | 25% | 100% |
Q91820 | Xenopus laevis | 25% | 100% |
Q9SLI2 | Arabidopsis thaliana | 27% | 78% |
Q9SN43 | Arabidopsis thaliana | 28% | 97% |
Q9UBS0 | Homo sapiens | 27% | 99% |
V5DC40 | Trypanosoma cruzi | 24% | 87% |
V5DFW9 | Trypanosoma cruzi | 28% | 82% |