A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8ICW9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 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 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.787 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.791 |
CLV_PCSK_PC7_1 | 32 | 38 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 580 | 586 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.592 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.729 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.576 |
DOC_CKS1_1 | 129 | 134 | PF01111 | 0.801 |
DOC_CKS1_1 | 495 | 500 | PF01111 | 0.385 |
DOC_MAPK_gen_1 | 452 | 461 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 390 | 397 | PF00149 | 0.409 |
DOC_PP1_RVXF_1 | 472 | 479 | PF00149 | 0.385 |
DOC_PP2B_PxIxI_1 | 594 | 600 | PF00149 | 0.351 |
DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.694 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.703 |
DOC_USP7_MATH_2 | 123 | 129 | PF00917 | 0.797 |
DOC_USP7_UBL2_3 | 470 | 474 | PF12436 | 0.273 |
DOC_USP7_UBL2_3 | 53 | 57 | PF12436 | 0.781 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.782 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.385 |
LIG_14-3-3_CanoR_1 | 134 | 139 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.487 |
LIG_APCC_ABBA_1 | 403 | 408 | PF00400 | 0.385 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.600 |
LIG_EVH1_2 | 227 | 231 | PF00568 | 0.732 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.809 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.510 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.385 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.487 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.680 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.385 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.385 |
LIG_LIR_Apic_2 | 119 | 123 | PF02991 | 0.693 |
LIG_LIR_Apic_2 | 497 | 503 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.385 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.385 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.385 |
LIG_SH3_2 | 536 | 541 | PF14604 | 0.385 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.795 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.810 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.385 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.741 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.635 |
LIG_SH3_4 | 53 | 60 | PF00018 | 0.670 |
LIG_SUMO_SIM_anti_2 | 234 | 239 | PF11976 | 0.675 |
LIG_SUMO_SIM_par_1 | 369 | 374 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 504 | 509 | PF11976 | 0.176 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.684 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.559 |
LIG_TRAF2_1 | 562 | 565 | PF00917 | 0.385 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.385 |
MOD_CDK_SPK_2 | 128 | 133 | PF00069 | 0.699 |
MOD_CDK_SPxK_1 | 128 | 134 | PF00069 | 0.677 |
MOD_CDK_SPxxK_3 | 128 | 135 | PF00069 | 0.802 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.656 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.594 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.685 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.486 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.385 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.402 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.669 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.699 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.571 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.385 |
MOD_GlcNHglycan | 112 | 116 | PF01048 | 0.708 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.659 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.650 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.553 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.393 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.316 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.487 |
MOD_GlcNHglycan | 507 | 511 | PF01048 | 0.385 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.385 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.385 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.385 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.700 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.803 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.744 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.715 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.614 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.664 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.572 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.403 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.487 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.385 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.385 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.385 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.351 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.385 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.788 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.507 |
MOD_N-GLC_2 | 387 | 389 | PF02516 | 0.385 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.577 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.742 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.493 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.385 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.385 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.684 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.385 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.630 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.626 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.445 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.307 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.382 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.341 |
MOD_PK_1 | 254 | 260 | PF00069 | 0.620 |
MOD_PKA_1 | 134 | 140 | PF00069 | 0.717 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.321 |
MOD_PKA_1 | 482 | 488 | PF00069 | 0.385 |
MOD_PKA_1 | 584 | 590 | PF00069 | 0.385 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.804 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.795 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.758 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.643 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.376 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.385 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.385 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.797 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.778 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.715 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.777 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.374 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.402 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.439 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.385 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.761 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.601 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.385 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 599 | 602 | PF00179 | 0.507 |
MOD_SUMO_rev_2 | 249 | 256 | PF00179 | 0.624 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.385 |
TRG_NES_CRM1_1 | 363 | 376 | PF08389 | 0.385 |
TRG_NLS_Bipartite_1 | 36 | 56 | PF00514 | 0.623 |
TRG_NLS_MonoCore_2 | 51 | 56 | PF00514 | 0.660 |
TRG_NLS_MonoExtC_3 | 419 | 424 | PF00514 | 0.385 |
TRG_NLS_MonoExtC_3 | 51 | 56 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 132 | 137 | PF00514 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTF0 | Leptomonas seymouri | 59% | 95% |
A0A3Q8ITZ9 | Leishmania donovani | 25% | 100% |
A4H459 | Leishmania braziliensis | 26% | 100% |
A4H601 | Leishmania braziliensis | 22% | 100% |
A4HDJ5 | Leishmania braziliensis | 80% | 100% |
A4HFA1 | Leishmania braziliensis | 25% | 100% |
A4HLJ9 | Leishmania braziliensis | 24% | 100% |
A4HSE2 | Leishmania infantum | 26% | 100% |
A4I0Y4 | Leishmania infantum | 100% | 100% |
A4I910 | Leishmania infantum | 25% | 100% |
E9AWZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B3X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q449 | Leishmania major | 25% | 100% |
Q4QAI6 | Leishmania major | 92% | 99% |
Q6F3A6 | Oryza sativa subsp. japonica | 26% | 100% |