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. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 21 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHQ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 34 |
GO:0006793 | phosphorus metabolic process | 3 | 34 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 34 |
GO:0006807 | nitrogen compound metabolic process | 2 | 34 |
GO:0008152 | metabolic process | 1 | 34 |
GO:0009987 | cellular process | 1 | 34 |
GO:0016310 | phosphorylation | 5 | 34 |
GO:0019538 | protein metabolic process | 3 | 34 |
GO:0036211 | protein modification process | 4 | 34 |
GO:0043170 | macromolecule metabolic process | 3 | 34 |
GO:0043412 | macromolecule modification | 4 | 34 |
GO:0044237 | cellular metabolic process | 2 | 34 |
GO:0044238 | primary metabolic process | 2 | 34 |
GO:0071704 | organic substance metabolic process | 2 | 34 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 34 |
GO:0003824 | catalytic activity | 1 | 34 |
GO:0004672 | protein kinase activity | 3 | 34 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 24 |
GO:0005488 | binding | 1 | 34 |
GO:0005524 | ATP binding | 5 | 34 |
GO:0016301 | kinase activity | 4 | 34 |
GO:0016740 | transferase activity | 2 | 34 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 34 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 34 |
GO:0017076 | purine nucleotide binding | 4 | 34 |
GO:0030554 | adenyl nucleotide binding | 5 | 34 |
GO:0032553 | ribonucleotide binding | 3 | 34 |
GO:0032555 | purine ribonucleotide binding | 4 | 34 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 34 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 34 |
GO:0036094 | small molecule binding | 2 | 34 |
GO:0043167 | ion binding | 2 | 34 |
GO:0043168 | anion binding | 3 | 34 |
GO:0097159 | organic cyclic compound binding | 2 | 34 |
GO:0097367 | carbohydrate derivative binding | 2 | 34 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 34 |
GO:1901265 | nucleoside phosphate binding | 3 | 34 |
GO:1901363 | heterocyclic compound binding | 2 | 34 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.283 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.292 |
CLV_PCSK_PC7_1 | 17 | 23 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.547 |
DOC_CYCLIN_yCln2_LP_2 | 219 | 225 | PF00134 | 0.322 |
DOC_MAPK_gen_1 | 147 | 156 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 17 | 25 | PF00069 | 0.212 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.355 |
DOC_USP7_MATH_2 | 248 | 254 | PF00917 | 0.432 |
DOC_USP7_UBL2_3 | 159 | 163 | PF12436 | 0.384 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.301 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.330 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.242 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.355 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.359 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.541 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.200 |
LIG_CtBP_PxDLS_1 | 248 | 252 | PF00389 | 0.322 |
LIG_deltaCOP1_diTrp_1 | 205 | 213 | PF00928 | 0.371 |
LIG_eIF4E_1 | 20 | 26 | PF01652 | 0.495 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.333 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.415 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.337 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.360 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.314 |
LIG_LIR_Apic_2 | 186 | 192 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.289 |
LIG_MAD2 | 234 | 242 | PF02301 | 0.287 |
LIG_MAD2 | 69 | 77 | PF02301 | 0.283 |
LIG_NRBOX | 227 | 233 | PF00104 | 0.307 |
LIG_PCNA_yPIPBox_3 | 473 | 483 | PF02747 | 0.402 |
LIG_PDZ_Class_2 | 501 | 506 | PF00595 | 0.502 |
LIG_PTB_Apo_2 | 10 | 17 | PF02174 | 0.312 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.261 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.342 |
LIG_SH2_NCK_1 | 240 | 244 | PF00017 | 0.283 |
LIG_SH2_SRC | 240 | 243 | PF00017 | 0.283 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 385 | 388 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.315 |
LIG_SH3_1 | 308 | 314 | PF00018 | 0.553 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.317 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.604 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.619 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.552 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.288 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.648 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.611 |
LIG_TYR_ITIM | 212 | 217 | PF00017 | 0.343 |
LIG_UBA3_1 | 341 | 349 | PF00899 | 0.587 |
LIG_WRC_WIRS_1 | 282 | 287 | PF05994 | 0.413 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.331 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.321 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.540 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.591 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.462 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.331 |
MOD_Cter_Amidation | 42 | 45 | PF01082 | 0.283 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.678 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.443 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.277 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.354 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.401 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.695 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.591 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.540 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.380 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.350 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.254 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.570 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.366 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.341 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.307 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.301 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.410 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.304 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.384 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.288 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.502 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.689 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.339 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.279 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.510 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.386 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.271 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.319 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.330 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.563 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.324 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.355 |
MOD_SUMO_rev_2 | 296 | 305 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 381 | 391 | PF00179 | 0.364 |
TRG_DiLeu_BaEn_1 | 475 | 480 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.327 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 9 | 14 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY86 | Leptomonas seymouri | 78% | 97% |
A0A0N1I9A0 | Leptomonas seymouri | 31% | 78% |
A0A0S4IKH2 | Bodo saltans | 68% | 100% |
A0A0S4J3Y5 | Bodo saltans | 27% | 100% |
A0A0S4J6L4 | Bodo saltans | 27% | 100% |
A0A0S4JIJ6 | Bodo saltans | 29% | 90% |
A0A0S4JN22 | Bodo saltans | 31% | 66% |
A0A0S4JNA1 | Bodo saltans | 37% | 100% |
A0A1X0NKF2 | Trypanosomatidae | 29% | 85% |
A0A1X0NTL6 | Trypanosomatidae | 29% | 100% |
A0A1X0NUB2 | Trypanosomatidae | 33% | 87% |
A0A1X0P9C4 | Trypanosomatidae | 73% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 38% | 100% |
A0A3Q8IB74 | Leishmania donovani | 26% | 100% |
A0A3Q8IC87 | Leishmania donovani | 28% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 39% | 100% |
A0A3Q8IHH8 | Leishmania donovani | 86% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 29% | 100% |
A0A3Q8INQ4 | Leishmania donovani | 26% | 100% |
A0A3R7RIN5 | Trypanosoma rangeli | 73% | 100% |
A0A3S5H5G0 | Leishmania donovani | 25% | 100% |
A0A3S7WWE7 | Leishmania donovani | 26% | 100% |
A0A3S7WYP4 | Leishmania donovani | 29% | 100% |
A0A3S7X2W3 | Leishmania donovani | 27% | 100% |
A0A3S7X5M4 | Leishmania donovani | 32% | 77% |
A0A3S7X7D5 | Leishmania donovani | 26% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 27% | 100% |
A0A3S7X9S2 | Leishmania donovani | 30% | 100% |
A0A422N3U8 | Trypanosoma rangeli | 28% | 70% |
A4HAS1 | Leishmania braziliensis | 28% | 100% |
A4HBL4 | Leishmania braziliensis | 24% | 100% |
A4HCE6 | Leishmania braziliensis | 37% | 100% |
A4HDU3 | Leishmania braziliensis | 30% | 100% |
A4HH03 | Leishmania braziliensis | 30% | 100% |
A4HHE4 | Leishmania braziliensis | 24% | 86% |
A4HHN1 | Leishmania braziliensis | 27% | 100% |
A4HJW2 | Leishmania braziliensis | 42% | 100% |
A4HKG9 | Leishmania braziliensis | 34% | 77% |
A4HLR0 | Leishmania braziliensis | 36% | 100% |
A4HSE2 | Leishmania infantum | 25% | 100% |
A4HZA2 | Leishmania infantum | 26% | 100% |
A4HZV1 | Leishmania infantum | 28% | 100% |
A4HZW8 | Leishmania infantum | 38% | 100% |
A4I140 | Leishmania infantum | 29% | 100% |
A4I1T4 | Leishmania infantum | 26% | 100% |
A4I435 | Leishmania infantum | 29% | 100% |
A4I4U6 | Leishmania infantum | 27% | 100% |
A4I4X0 | Leishmania infantum | 87% | 100% |
A4I7A1 | Leishmania infantum | 39% | 100% |
A4I7Z6 | Leishmania infantum | 32% | 77% |
A4I9H1 | Leishmania infantum | 26% | 100% |
A4I9Y5 | Leishmania infantum | 27% | 100% |
D0A118 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 66% |
E9AEB9 | Leishmania major | 86% | 100% |
E9AFM1 | Leishmania major | 30% | 100% |
E9ALG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9ARW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AX78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B2V8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 77% |
E9B4G9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
O08875 | Rattus norvegicus | 28% | 100% |
P87248 | Colletotrichum lindemuthianum | 29% | 75% |
Q4Q1S4 | Leishmania major | 29% | 100% |
Q4Q2Z2 | Leishmania major | 27% | 100% |
Q4Q598 | Leishmania major | 33% | 77% |
Q4Q5W2 | Leishmania major | 39% | 100% |
Q4Q7W2 | Leishmania major | 29% | 100% |
Q4Q9K2 | Leishmania major | 26% | 100% |
Q4QA98 | Leishmania major | 28% | 100% |
Q4QBQ2 | Leishmania major | 38% | 100% |
Q4QBR6 | Leishmania major | 28% | 100% |
Q4QCK0 | Leishmania major | 24% | 100% |
Q4QJJ0 | Leishmania major | 26% | 100% |
Q63553 | Rattus norvegicus | 26% | 68% |
Q8C0Q4 | Mus musculus | 30% | 81% |
Q8INB9 | Drosophila melanogaster | 27% | 83% |
Q9SN43 | Arabidopsis thaliana | 27% | 100% |
Q9Y077 | Leishmania major | 27% | 100% |
V5BHW8 | Trypanosoma cruzi | 29% | 80% |
V5BLW4 | Trypanosoma cruzi | 44% | 66% |
V5C224 | Trypanosoma cruzi | 73% | 100% |
V5DFW9 | Trypanosoma cruzi | 33% | 87% |