Protein kinase, Uncharacterized
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) | yes | yes: 3 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HVK6
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: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 | 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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 487 | 491 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 660 | 662 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.410 |
CLV_Separin_Metazoa | 604 | 608 | PF03568 | 0.310 |
DEG_APCC_DBOX_1 | 676 | 684 | PF00400 | 0.408 |
DEG_COP1_1 | 656 | 665 | PF00400 | 0.497 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.502 |
DEG_ODPH_VHL_1 | 288 | 301 | PF01847 | 0.467 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.500 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.606 |
DEG_SPOP_SBC_1 | 390 | 394 | PF00917 | 0.628 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.470 |
DOC_CYCLIN_RxL_1 | 200 | 207 | PF00134 | 0.406 |
DOC_CYCLIN_RxL_1 | 534 | 544 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 368 | 374 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 120 | 126 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 450 | 459 | PF00069 | 0.337 |
DOC_MAPK_RevD_3 | 107 | 121 | PF00069 | 0.516 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.383 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.356 |
DOC_USP7_UBL2_3 | 586 | 590 | PF12436 | 0.337 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.293 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.503 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.395 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.484 |
LIG_EH_1 | 640 | 644 | PF12763 | 0.365 |
LIG_eIF4E_1 | 191 | 197 | PF01652 | 0.404 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.557 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.438 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.431 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.396 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.613 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.537 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.260 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.570 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.413 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.413 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.536 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.403 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.444 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.638 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.374 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.310 |
LIG_LIR_Apic_2 | 236 | 241 | PF02991 | 0.389 |
LIG_LIR_Apic_2 | 493 | 499 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 135 | 145 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 249 | 256 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 693 | 700 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 647 | 652 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 693 | 698 | PF02991 | 0.471 |
LIG_NRBOX | 135 | 141 | PF00104 | 0.480 |
LIG_NRBOX | 601 | 607 | PF00104 | 0.310 |
LIG_PTB_Apo_2 | 638 | 645 | PF02174 | 0.337 |
LIG_REV1ctd_RIR_1 | 641 | 650 | PF16727 | 0.505 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.486 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.420 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.421 |
LIG_SH2_CRK | 649 | 653 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 177 | 181 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 496 | 500 | PF00017 | 0.337 |
LIG_SH2_SRC | 177 | 180 | PF00017 | 0.470 |
LIG_SH2_SRC | 649 | 652 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.337 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.564 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.494 |
LIG_SH3_3 | 649 | 655 | PF00018 | 0.579 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 51 | 60 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 500 | 508 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 51 | 60 | PF11976 | 0.491 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.549 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.468 |
LIG_TYR_ITIM | 11 | 16 | PF00017 | 0.492 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.327 |
MOD_CDK_SPxK_1 | 315 | 321 | PF00069 | 0.587 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.729 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.515 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.337 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.506 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.405 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.546 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.401 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.454 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.739 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.408 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.310 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.496 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.379 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.389 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.694 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.519 |
MOD_GlcNHglycan | 560 | 564 | PF01048 | 0.336 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.434 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.574 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.545 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.435 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.727 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.603 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.772 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.520 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.377 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.487 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.305 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.316 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.591 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.474 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.416 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.274 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.393 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.444 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.567 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.337 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.524 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.337 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.374 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.375 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.496 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.441 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.503 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.509 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.357 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.365 |
MOD_PK_1 | 661 | 667 | PF00069 | 0.529 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.693 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.636 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.370 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.337 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.502 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.537 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.589 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.401 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.444 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.337 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.367 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.507 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.490 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.567 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.399 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.420 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.628 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.405 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.337 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.498 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.337 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.472 |
MOD_Plk_4 | 694 | 700 | PF00069 | 0.476 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.478 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.513 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.660 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.467 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.388 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.293 |
MOD_SUMO_for_1 | 327 | 330 | PF00179 | 0.595 |
MOD_SUMO_for_1 | 452 | 455 | PF00179 | 0.337 |
MOD_SUMO_for_1 | 700 | 703 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 686 | 694 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 703 | 708 | PF00179 | 0.462 |
TRG_DiLeu_BaEn_1 | 135 | 140 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 1 | 6 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.401 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 649 | 652 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.520 |
TRG_ER_FFAT_1 | 175 | 183 | PF00635 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 450 | 455 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.337 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZJ0 | Leptomonas seymouri | 71% | 100% |
A0A3Q8I9M4 | Leishmania donovani | 100% | 100% |
A4H767 | Leishmania braziliensis | 82% | 100% |
E9APA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 94% |
Q4QG76 | Leishmania major | 89% | 92% |