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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 33 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 81 |
NetGPI | no | yes: 0, no: 81 |
Related structures:
AlphaFold database: E9B745
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 82 |
GO:0006793 | phosphorus metabolic process | 3 | 82 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 82 |
GO:0006807 | nitrogen compound metabolic process | 2 | 82 |
GO:0008152 | metabolic process | 1 | 82 |
GO:0009987 | cellular process | 1 | 82 |
GO:0016310 | phosphorylation | 5 | 82 |
GO:0019538 | protein metabolic process | 3 | 82 |
GO:0036211 | protein modification process | 4 | 82 |
GO:0043170 | macromolecule metabolic process | 3 | 82 |
GO:0043412 | macromolecule modification | 4 | 82 |
GO:0044237 | cellular metabolic process | 2 | 82 |
GO:0044238 | primary metabolic process | 2 | 82 |
GO:0071704 | organic substance metabolic process | 2 | 82 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 82 |
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 | 82 |
GO:0003824 | catalytic activity | 1 | 82 |
GO:0004672 | protein kinase activity | 3 | 82 |
GO:0005488 | binding | 1 | 82 |
GO:0005524 | ATP binding | 5 | 82 |
GO:0016301 | kinase activity | 4 | 82 |
GO:0016740 | transferase activity | 2 | 82 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 82 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 82 |
GO:0017076 | purine nucleotide binding | 4 | 82 |
GO:0030554 | adenyl nucleotide binding | 5 | 82 |
GO:0032553 | ribonucleotide binding | 3 | 82 |
GO:0032555 | purine ribonucleotide binding | 4 | 82 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 82 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 82 |
GO:0036094 | small molecule binding | 2 | 82 |
GO:0043167 | ion binding | 2 | 82 |
GO:0043168 | anion binding | 3 | 82 |
GO:0097159 | organic cyclic compound binding | 2 | 82 |
GO:0097367 | carbohydrate derivative binding | 2 | 82 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 82 |
GO:1901265 | nucleoside phosphate binding | 3 | 82 |
GO:1901363 | heterocyclic compound binding | 2 | 82 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 49 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.277 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.314 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.418 |
DEG_APCC_KENBOX_2 | 160 | 164 | PF00400 | 0.135 |
DEG_COP1_1 | 425 | 436 | PF00400 | 0.342 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.160 |
DOC_CDC14_PxL_1 | 236 | 244 | PF14671 | 0.299 |
DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 135 | 144 | PF00069 | 0.258 |
DOC_MAPK_MEF2A_6 | 21 | 28 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 440 | 449 | PF00069 | 0.380 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.305 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.305 |
DOC_PP4_FxxP_1 | 291 | 294 | PF00568 | 0.328 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.264 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.282 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.284 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.243 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 314 | 321 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.444 |
LIG_AP2alpha_2 | 289 | 291 | PF02296 | 0.272 |
LIG_APCC_ABBAyCdc20_2 | 188 | 194 | PF00400 | 0.313 |
LIG_Clathr_ClatBox_1 | 141 | 145 | PF01394 | 0.256 |
LIG_deltaCOP1_diTrp_1 | 389 | 397 | PF00928 | 0.280 |
LIG_deltaCOP1_diTrp_1 | 466 | 472 | PF00928 | 0.366 |
LIG_eIF4E_1 | 169 | 175 | PF01652 | 0.341 |
LIG_eIF4E_1 | 22 | 28 | PF01652 | 0.463 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.383 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.542 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.276 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.308 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.511 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.527 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.434 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.419 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.337 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.293 |
LIG_HCF-1_HBM_1 | 66 | 69 | PF13415 | 0.529 |
LIG_LIR_Apic_2 | 234 | 240 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 289 | 294 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 429 | 434 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.383 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.249 |
LIG_Pex14_1 | 392 | 396 | PF04695 | 0.281 |
LIG_Pex14_1 | 468 | 472 | PF04695 | 0.340 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 458 | 461 | PF00017 | 0.155 |
LIG_SH2_GRB2like | 46 | 49 | PF00017 | 0.418 |
LIG_SH2_SRC | 176 | 179 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.371 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.599 |
LIG_SUMO_SIM_anti_2 | 136 | 145 | PF11976 | 0.255 |
LIG_SUMO_SIM_par_1 | 136 | 145 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.237 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.380 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.558 |
LIG_TRFH_1 | 236 | 240 | PF08558 | 0.275 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.310 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.320 |
LIG_UBA3_1 | 264 | 272 | PF00899 | 0.297 |
LIG_UBA3_1 | 302 | 309 | PF00899 | 0.304 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.558 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.478 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.354 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.610 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.306 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.437 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.388 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.289 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.265 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.317 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.583 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.605 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.270 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.304 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.319 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.427 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.557 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.564 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.294 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.281 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.434 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.349 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.249 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.541 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.389 |
MOD_PKA_1 | 246 | 252 | PF00069 | 0.314 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.309 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.299 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.396 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.339 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.416 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.603 |
MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.282 |
MOD_Plk_2-3 | 221 | 227 | PF00069 | 0.307 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.437 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.305 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.673 |
MOD_SUMO_rev_2 | 132 | 141 | PF00179 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 302 | 307 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.276 |
TRG_NLS_MonoExtN_4 | 391 | 397 | PF00514 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 39% | 100% |
A0A0N0P953 | Leptomonas seymouri | 87% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 27% | 74% |
A0A0N1PD05 | Leptomonas seymouri | 36% | 100% |
A0A0S4IMB7 | Bodo saltans | 37% | 100% |
A0A0S4IQ75 | Bodo saltans | 29% | 95% |
A0A0S4IRZ7 | Bodo saltans | 35% | 97% |
A0A0S4IVW1 | Bodo saltans | 28% | 76% |
A0A0S4IX86 | Bodo saltans | 38% | 100% |
A0A0S4J575 | Bodo saltans | 27% | 77% |
A0A0S4J804 | Bodo saltans | 64% | 91% |
A0A0S4JIJ6 | Bodo saltans | 31% | 85% |
A0A0S4JPZ1 | Bodo saltans | 34% | 100% |
A0A0S4JQN5 | Bodo saltans | 29% | 68% |
A0A1X0NIA0 | Trypanosomatidae | 39% | 100% |
A0A1X0NIX2 | Trypanosomatidae | 34% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 32% | 82% |
A0A1X0P527 | Trypanosomatidae | 37% | 100% |
A0A1X0P549 | Trypanosomatidae | 74% | 100% |
A0A1X0P863 | Trypanosomatidae | 37% | 96% |
A0A1X0P994 | Trypanosomatidae | 35% | 96% |
A0A3Q8IAQ1 | Leishmania donovani | 35% | 100% |
A0A3Q8IC87 | Leishmania donovani | 30% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 38% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 31% | 100% |
A0A3Q8IJM9 | Leishmania donovani | 96% | 100% |
A0A3R7KCZ4 | Trypanosoma rangeli | 40% | 100% |
A0A3R7MKG5 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X2W9 | Leishmania donovani | 25% | 100% |
A0A3S7X5M4 | Leishmania donovani | 30% | 73% |
A0A3S7X6T8 | Leishmania donovani | 35% | 100% |
A0A3S7XAL3 | Leishmania donovani | 35% | 96% |
A0A3S7XAT9 | Leishmania donovani | 36% | 95% |
A0A422NCP0 | Trypanosoma rangeli | 36% | 96% |
A0A422NH41 | Trypanosoma rangeli | 33% | 83% |
A4H4S9 | Leishmania braziliensis | 26% | 100% |
A4HED7 | Leishmania braziliensis | 30% | 100% |
A4HH03 | Leishmania braziliensis | 28% | 100% |
A4HJT5 | Leishmania braziliensis | 35% | 100% |
A4HJW2 | Leishmania braziliensis | 37% | 100% |
A4HKG9 | Leishmania braziliensis | 29% | 100% |
A4HLR0 | Leishmania braziliensis | 35% | 100% |
A4HNI1 | Leishmania braziliensis | 90% | 100% |
A4HP12 | Leishmania braziliensis | 34% | 100% |
A4HP13 | Leishmania braziliensis | 36% | 100% |
A4HZV1 | Leishmania infantum | 30% | 100% |
A4HZW8 | Leishmania infantum | 35% | 100% |
A4I435 | Leishmania infantum | 31% | 100% |
A4I4Y0 | Leishmania infantum | 25% | 100% |
A4I7C4 | Leishmania infantum | 38% | 100% |
A4I7Z6 | Leishmania infantum | 30% | 73% |
A4I960 | Leishmania infantum | 35% | 100% |
A4IC37 | Leishmania infantum | 96% | 100% |
A4IDC1 | Leishmania infantum | 34% | 94% |
A4IDC2 | Leishmania infantum | 36% | 95% |
C9ZMH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZWK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A2Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 98% |
D0A2Z6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 97% |
D0AA64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 83% |
E9AED4 | Leishmania major | 25% | 100% |
E9AFZ2 | Leishmania major | 96% | 100% |
E9ASS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ASS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 73% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q03428 | Trypanosoma brucei brucei | 38% | 100% |
Q08942 | Trypanosoma brucei brucei | 39% | 100% |
Q12469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 73% |
Q4Q1S3 | Leishmania major | 38% | 100% |
Q4Q1S4 | Leishmania major | 34% | 100% |
Q4Q3Y9 | Leishmania major | 35% | 100% |
Q4Q598 | Leishmania major | 29% | 100% |
Q4Q5T9 | Leishmania major | 38% | 100% |
Q4Q5W2 | Leishmania major | 35% | 100% |
Q4Q7W2 | Leishmania major | 31% | 100% |
Q4QBQ2 | Leishmania major | 40% | 100% |
Q4QBR6 | Leishmania major | 30% | 100% |
Q4QCK0 | Leishmania major | 23% | 100% |
Q4QIV8 | Leishmania major | 25% | 100% |
V5BC28 | Trypanosoma cruzi | 38% | 95% |
V5BPJ0 | Trypanosoma cruzi | 36% | 97% |
V5D579 | Trypanosoma cruzi | 39% | 100% |
V5DFW9 | Trypanosoma cruzi | 31% | 82% |