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: 5 |
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: 19 |
NetGPI | no | yes: 0, no: 19 |
Related structures:
AlphaFold database: E9AT06
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 20 |
GO:0006793 | phosphorus metabolic process | 3 | 20 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 20 |
GO:0006807 | nitrogen compound metabolic process | 2 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0009987 | cellular process | 1 | 20 |
GO:0016310 | phosphorylation | 5 | 20 |
GO:0019538 | protein metabolic process | 3 | 20 |
GO:0036211 | protein modification process | 4 | 20 |
GO:0043170 | macromolecule metabolic process | 3 | 20 |
GO:0043412 | macromolecule modification | 4 | 20 |
GO:0044237 | cellular metabolic process | 2 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 20 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0004672 | protein kinase activity | 3 | 20 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 19 |
GO:0005488 | binding | 1 | 20 |
GO:0005524 | ATP binding | 5 | 20 |
GO:0016301 | kinase activity | 4 | 20 |
GO:0016740 | transferase activity | 2 | 20 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 20 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 20 |
GO:0017076 | purine nucleotide binding | 4 | 20 |
GO:0030554 | adenyl nucleotide binding | 5 | 20 |
GO:0032553 | ribonucleotide binding | 3 | 20 |
GO:0032555 | purine ribonucleotide binding | 4 | 20 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 20 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 20 |
GO:0036094 | small molecule binding | 2 | 20 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043168 | anion binding | 3 | 20 |
GO:0097159 | organic cyclic compound binding | 2 | 20 |
GO:0097367 | carbohydrate derivative binding | 2 | 20 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 20 |
GO:1901265 | nucleoside phosphate binding | 3 | 20 |
GO:1901363 | heterocyclic compound binding | 2 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 125 | 131 | PF00082 | 0.428 |
CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.362 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.337 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 329 | 335 | PF00134 | 0.335 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.480 |
DOC_MAPK_gen_1 | 464 | 474 | PF00069 | 0.577 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.600 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 288 | 297 | PF00244 | 0.211 |
LIG_14-3-3_CanoR_1 | 309 | 313 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.348 |
LIG_BIR_III_4 | 66 | 70 | PF00653 | 0.467 |
LIG_Clathr_ClatBox_1 | 203 | 207 | PF01394 | 0.359 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.273 |
LIG_eIF4E_1 | 95 | 101 | PF01652 | 0.463 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.371 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.331 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.262 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.210 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.512 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.311 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.363 |
LIG_Integrin_RGD_1 | 306 | 308 | PF01839 | 0.208 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.319 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 232 | 243 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 349 | 357 | PF02991 | 0.214 |
LIG_LIR_Gen_1 | 363 | 373 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 413 | 422 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.313 |
LIG_MYND_1 | 56 | 60 | PF01753 | 0.506 |
LIG_NRBOX | 322 | 328 | PF00104 | 0.205 |
LIG_Pex14_1 | 441 | 445 | PF04695 | 0.518 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.655 |
LIG_PTB_Apo_2 | 344 | 351 | PF02174 | 0.184 |
LIG_PTB_Phospho_1 | 344 | 350 | PF10480 | 0.184 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.208 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.208 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.278 |
LIG_SH2_GRB2like | 357 | 360 | PF00017 | 0.219 |
LIG_SH2_SRC | 445 | 448 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.184 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.480 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.466 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.440 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.546 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.660 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 325 | 330 | PF11976 | 0.208 |
LIG_SUMO_SIM_par_1 | 367 | 372 | PF11976 | 0.274 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.430 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.338 |
LIG_TRFH_1 | 298 | 302 | PF08558 | 0.313 |
LIG_TYR_ITAM | 347 | 369 | PF00017 | 0.184 |
LIG_TYR_ITIM | 322 | 327 | PF00017 | 0.317 |
LIG_TYR_ITIM | 364 | 369 | PF00017 | 0.208 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.484 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.273 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.452 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.457 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.593 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.256 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.232 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.620 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.473 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.550 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.483 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.772 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.334 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.302 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.168 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.589 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.427 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.520 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.489 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.550 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.358 |
MOD_N-GLC_2 | 479 | 481 | PF02516 | 0.453 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.307 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.284 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.555 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.580 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.459 |
MOD_PK_1 | 2 | 8 | PF00069 | 0.478 |
MOD_PK_1 | 71 | 77 | PF00069 | 0.449 |
MOD_PKA_1 | 279 | 285 | PF00069 | 0.189 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.324 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.364 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.330 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.324 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.395 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.490 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.504 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.181 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.353 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.419 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.472 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.253 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.343 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.583 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.208 |
MOD_SUMO_for_1 | 312 | 315 | PF00179 | 0.208 |
MOD_SUMO_rev_2 | 403 | 413 | PF00179 | 0.395 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.230 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.248 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.231 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A0 | Leptomonas seymouri | 28% | 74% |
A0A0S4IRZ7 | Bodo saltans | 30% | 98% |
A0A1X0NIA0 | Trypanosomatidae | 35% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 29% | 83% |
A0A3Q8IAQ1 | Leishmania donovani | 41% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 35% | 100% |
A0A3S7XAX0 | Leishmania donovani | 89% | 100% |
A0A422P4V9 | Trypanosoma rangeli | 26% | 100% |
A4H7V0 | Leishmania braziliensis | 25% | 67% |
A4HCE6 | Leishmania braziliensis | 39% | 100% |
A4HI35 | Leishmania braziliensis | 25% | 94% |
A4HJT5 | Leishmania braziliensis | 39% | 100% |
A4HZW8 | Leishmania infantum | 41% | 100% |
A4I7A1 | Leishmania infantum | 35% | 100% |
A4IDK3 | Leishmania infantum | 90% | 100% |
A5GFW1 | Sus scrofa | 27% | 100% |
C9ZTU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 88% |
D0A7M4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 84% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 67% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 73% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B6S4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B6S9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
O00141 | Homo sapiens | 27% | 100% |
O14965 | Homo sapiens | 27% | 100% |
O59790 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
P28178 | Dictyostelium discoideum | 27% | 100% |
P59241 | Rattus norvegicus | 27% | 100% |
P97477 | Mus musculus | 26% | 100% |
Q10056 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 82% |
Q2TA06 | Bos taurus | 27% | 100% |
Q4Q1J2 | Leishmania major | 88% | 99% |
Q4Q5W2 | Leishmania major | 40% | 100% |
Q4Q7M5 | Leishmania major | 25% | 94% |
Q4QBQ2 | Leishmania major | 40% | 100% |
Q4QFK4 | Leishmania major | 25% | 77% |
Q4R633 | Macaca fascicularis | 27% | 100% |
Q5Q0U5 | Fundulus heteroclitus | 28% | 100% |
Q6U1I9 | Gallus gallus | 27% | 100% |
Q869W6 | Dictyostelium discoideum | 29% | 100% |
Q8NG66 | Homo sapiens | 29% | 75% |
Q91820 | Xenopus laevis | 26% | 100% |
Q9NAH6 | Caenorhabditis elegans | 25% | 87% |
V5B9Y9 | Trypanosoma cruzi | 24% | 100% |