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: 6 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 42 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 77 |
NetGPI | no | yes: 0, no: 77 |
Related structures:
AlphaFold database: A4IC37
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 78 |
GO:0006793 | phosphorus metabolic process | 3 | 78 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 78 |
GO:0006807 | nitrogen compound metabolic process | 2 | 78 |
GO:0008152 | metabolic process | 1 | 78 |
GO:0009987 | cellular process | 1 | 78 |
GO:0016310 | phosphorylation | 5 | 78 |
GO:0019538 | protein metabolic process | 3 | 78 |
GO:0036211 | protein modification process | 4 | 78 |
GO:0043170 | macromolecule metabolic process | 3 | 78 |
GO:0043412 | macromolecule modification | 4 | 78 |
GO:0044237 | cellular metabolic process | 2 | 78 |
GO:0044238 | primary metabolic process | 2 | 78 |
GO:0071704 | organic substance metabolic process | 2 | 78 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 78 |
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 | 78 |
GO:0003824 | catalytic activity | 1 | 78 |
GO:0004672 | protein kinase activity | 3 | 78 |
GO:0005488 | binding | 1 | 78 |
GO:0005524 | ATP binding | 5 | 78 |
GO:0016301 | kinase activity | 4 | 78 |
GO:0016740 | transferase activity | 2 | 78 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 78 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 78 |
GO:0017076 | purine nucleotide binding | 4 | 78 |
GO:0030554 | adenyl nucleotide binding | 5 | 78 |
GO:0032553 | ribonucleotide binding | 3 | 78 |
GO:0032555 | purine ribonucleotide binding | 4 | 78 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 78 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 78 |
GO:0036094 | small molecule binding | 2 | 78 |
GO:0043167 | ion binding | 2 | 78 |
GO:0043168 | anion binding | 3 | 78 |
GO:0097159 | organic cyclic compound binding | 2 | 78 |
GO:0097367 | carbohydrate derivative binding | 2 | 78 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 78 |
GO:1901265 | nucleoside phosphate binding | 3 | 78 |
GO:1901363 | heterocyclic compound binding | 2 | 78 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 50 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.266 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.305 |
CLV_Separin_Metazoa | 349 | 353 | PF03568 | 0.452 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.410 |
DEG_COP1_1 | 424 | 435 | PF00400 | 0.333 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.161 |
DOC_CDC14_PxL_1 | 235 | 243 | PF14671 | 0.290 |
DOC_MAPK_gen_1 | 156 | 165 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 192 | 201 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 134 | 143 | PF00069 | 0.290 |
DOC_MAPK_MEF2A_6 | 21 | 28 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 439 | 448 | PF00069 | 0.350 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.295 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.295 |
DOC_PP4_FxxP_1 | 290 | 293 | PF00568 | 0.266 |
DOC_PP4_FxxP_1 | 430 | 433 | PF00568 | 0.260 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.273 |
DOC_USP7_UBL2_3 | 156 | 160 | PF12436 | 0.283 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.241 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 106 | 111 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 313 | 320 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 337 | 344 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 76 | 84 | PF00244 | 0.438 |
LIG_AP2alpha_2 | 288 | 290 | PF02296 | 0.263 |
LIG_APCC_ABBAyCdc20_2 | 187 | 193 | PF00400 | 0.311 |
LIG_Clathr_ClatBox_1 | 140 | 144 | PF01394 | 0.252 |
LIG_deltaCOP1_diTrp_1 | 388 | 396 | PF00928 | 0.289 |
LIG_deltaCOP1_diTrp_1 | 465 | 471 | PF00928 | 0.357 |
LIG_eIF4E_1 | 168 | 174 | PF01652 | 0.351 |
LIG_eIF4E_1 | 22 | 28 | PF01652 | 0.404 |
LIG_eIF4E_1 | 68 | 74 | PF01652 | 0.371 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.470 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.277 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.322 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.509 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.464 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.447 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.359 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.337 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.294 |
LIG_HCF-1_HBM_1 | 65 | 68 | PF13415 | 0.499 |
LIG_LIR_Apic_2 | 233 | 239 | PF02991 | 0.307 |
LIG_LIR_Apic_2 | 288 | 293 | PF02991 | 0.298 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.389 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.245 |
LIG_Pex14_1 | 391 | 395 | PF04695 | 0.271 |
LIG_Pex14_1 | 467 | 471 | PF04695 | 0.331 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 457 | 460 | PF00017 | 0.155 |
LIG_SH2_SRC | 175 | 178 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.368 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 135 | 144 | PF11976 | 0.247 |
LIG_SUMO_SIM_par_1 | 135 | 144 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.239 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.379 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.268 |
LIG_TYR_ITIM | 173 | 178 | PF00017 | 0.300 |
LIG_TYR_ITIM | 259 | 264 | PF00017 | 0.318 |
LIG_UBA3_1 | 263 | 271 | PF00899 | 0.284 |
LIG_UBA3_1 | 301 | 308 | PF00899 | 0.300 |
MOD_CDK_SPxxK_3 | 340 | 347 | PF00069 | 0.288 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.436 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.480 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.352 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.300 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.407 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.385 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.296 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.264 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.339 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.346 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.613 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.334 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.303 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.304 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.450 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.533 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.323 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.280 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.294 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.422 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.329 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.246 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.491 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.330 |
MOD_PKA_1 | 245 | 251 | PF00069 | 0.349 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.311 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.299 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.386 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.339 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.396 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.273 |
MOD_Plk_2-3 | 220 | 226 | PF00069 | 0.295 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.466 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.308 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.525 |
MOD_SUMO_rev_2 | 131 | 140 | PF00179 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.285 |
TRG_NLS_MonoExtN_4 | 390 | 396 | PF00514 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 38% | 100% |
A0A0N0P953 | Leptomonas seymouri | 88% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 28% | 73% |
A0A0N1PD05 | Leptomonas seymouri | 36% | 100% |
A0A0S4IMB7 | Bodo saltans | 38% | 100% |
A0A0S4IQ75 | Bodo saltans | 30% | 95% |
A0A0S4IRZ7 | Bodo saltans | 35% | 97% |
A0A0S4IVW1 | Bodo saltans | 29% | 76% |
A0A0S4IX86 | Bodo saltans | 38% | 100% |
A0A0S4J804 | Bodo saltans | 64% | 91% |
A0A0S4JIJ6 | Bodo saltans | 25% | 84% |
A0A0S4JPZ1 | Bodo saltans | 35% | 100% |
A0A1X0NIA0 | Trypanosomatidae | 39% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 34% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 32% | 82% |
A0A1X0P527 | Trypanosomatidae | 38% | 100% |
A0A1X0P549 | Trypanosomatidae | 75% | 100% |
A0A1X0P863 | Trypanosomatidae | 36% | 96% |
A0A1X0P994 | Trypanosomatidae | 34% | 96% |
A0A3Q8IAQ1 | Leishmania donovani | 38% | 100% |
A0A3Q8IC87 | Leishmania donovani | 30% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 38% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 99% | 100% |
A0A3Q8INQ4 | Leishmania donovani | 31% | 100% |
A0A3R7KCZ4 | Trypanosoma rangeli | 40% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 37% | 100% |
A0A3S5H5U5 | Leishmania donovani | 25% | 100% |
A0A3S7X5M4 | Leishmania donovani | 29% | 73% |
A0A3S7X6T8 | Leishmania donovani | 35% | 100% |
A0A3S7XAL3 | Leishmania donovani | 36% | 96% |
A0A3S7XAT9 | Leishmania donovani | 36% | 95% |
A0A422NCP0 | Trypanosoma rangeli | 36% | 96% |
A0A422NH41 | Trypanosoma rangeli | 33% | 83% |
A4H4S9 | Leishmania braziliensis | 25% | 100% |
A4HED7 | Leishmania braziliensis | 31% | 100% |
A4HH03 | Leishmania braziliensis | 28% | 100% |
A4HJT5 | Leishmania braziliensis | 36% | 100% |
A4HJW2 | Leishmania braziliensis | 37% | 100% |
A4HKG9 | Leishmania braziliensis | 29% | 100% |
A4HLR0 | Leishmania braziliensis | 36% | 100% |
A4HNI1 | Leishmania braziliensis | 90% | 100% |
A4HP12 | Leishmania braziliensis | 35% | 100% |
A4HP13 | Leishmania braziliensis | 36% | 100% |
A4HZV1 | Leishmania infantum | 30% | 100% |
A4HZW8 | Leishmania infantum | 38% | 100% |
A4I1T4 | Leishmania infantum | 31% | 100% |
A4I7C4 | Leishmania infantum | 38% | 100% |
A4I7Z6 | Leishmania infantum | 29% | 100% |
A4I960 | Leishmania infantum | 35% | 100% |
A4IDC1 | Leishmania infantum | 35% | 94% |
A4IDC2 | Leishmania infantum | 36% | 95% |
C9ZMH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 97% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 97% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 83% |
E9AFZ2 | Leishmania major | 97% | 100% |
E9AG71 | Leishmania infantum | 25% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 73% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B745 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P49071 | Drosophila melanogaster | 28% | 100% |
Q00771 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
Q03428 | Trypanosoma brucei brucei | 38% | 100% |
Q08942 | Trypanosoma brucei brucei | 39% | 100% |
Q4Q1S3 | Leishmania major | 38% | 100% |
Q4Q1S4 | Leishmania major | 34% | 100% |
Q4Q3Y9 | Leishmania major | 35% | 100% |
Q4Q598 | Leishmania major | 30% | 100% |
Q4Q5T9 | Leishmania major | 38% | 100% |
Q4Q7W2 | Leishmania major | 31% | 100% |
Q4QBQ2 | Leishmania major | 41% | 100% |
Q4QBR6 | Leishmania major | 30% | 100% |
Q4QCK0 | Leishmania major | 23% | 100% |
V5BC28 | Trypanosoma cruzi | 39% | 95% |
V5BPJ0 | Trypanosoma cruzi | 36% | 96% |
V5D579 | Trypanosoma cruzi | 39% | 100% |
V5DFW9 | Trypanosoma cruzi | 32% | 82% |
V5DKY9 | Trypanosoma cruzi | 27% | 77% |