Protein kinase, kinase, putative
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HWH3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0004713 | protein tyrosine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.578 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.229 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.229 |
CLV_PCSK_PC1ET2_1 | 651 | 653 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.229 |
CLV_PCSK_PC7_1 | 647 | 653 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.229 |
DEG_APCC_KENBOX_2 | 293 | 297 | PF00400 | 0.210 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.578 |
DOC_CYCLIN_RxL_1 | 83 | 96 | PF00134 | 0.260 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.325 |
DOC_MAPK_gen_1 | 194 | 203 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.248 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.219 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.273 |
DOC_PP4_FxxP_1 | 625 | 628 | PF00568 | 0.672 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.222 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.562 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 151 | 161 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 647 | 655 | PF00244 | 0.568 |
LIG_AP2alpha_1 | 500 | 504 | PF02296 | 0.527 |
LIG_AP2alpha_1 | 655 | 659 | PF02296 | 0.569 |
LIG_AP2alpha_2 | 256 | 258 | PF02296 | 0.360 |
LIG_AP2alpha_2 | 653 | 655 | PF02296 | 0.517 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.757 |
LIG_deltaCOP1_diTrp_1 | 295 | 301 | PF00928 | 0.340 |
LIG_deltaCOP1_diTrp_1 | 357 | 362 | PF00928 | 0.451 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.246 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.255 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.684 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.342 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.360 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.342 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.360 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.470 |
LIG_Integrin_isoDGR_2 | 417 | 419 | PF01839 | 0.571 |
LIG_LIR_Apic_2 | 382 | 386 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 623 | 628 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 498 | 507 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 653 | 659 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.248 |
LIG_LYPXL_yS_3 | 555 | 558 | PF13949 | 0.571 |
LIG_MAD2 | 368 | 376 | PF02301 | 0.566 |
LIG_MYND_1 | 549 | 553 | PF01753 | 0.526 |
LIG_Pex14_1 | 297 | 301 | PF04695 | 0.360 |
LIG_Pex14_2 | 500 | 504 | PF04695 | 0.527 |
LIG_Pex14_2 | 655 | 659 | PF04695 | 0.525 |
LIG_PTAP_UEV_1 | 522 | 527 | PF05743 | 0.599 |
LIG_PTB_Apo_2 | 243 | 250 | PF02174 | 0.342 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.273 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.618 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.652 |
LIG_SH2_NCK_1 | 608 | 612 | PF00017 | 0.677 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.248 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.235 |
LIG_SH2_SRC | 608 | 611 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.303 |
LIG_SH2_STAT3 | 585 | 588 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.248 |
LIG_SH3_1 | 608 | 614 | PF00018 | 0.564 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.377 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.402 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.450 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.574 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.676 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.434 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.616 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.609 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.625 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.316 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 34 | 41 | PF11976 | 0.315 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.360 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.583 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.664 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.394 |
LIG_WW_1 | 54 | 57 | PF00397 | 0.509 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.272 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.325 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.368 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.557 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.421 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.286 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.360 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.393 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.447 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.596 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.459 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.351 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.309 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.593 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.531 |
MOD_GlcNHglycan | 481 | 485 | PF01048 | 0.689 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.627 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.741 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.622 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.594 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.597 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.559 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.313 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.377 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.419 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.519 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.634 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.692 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.627 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.351 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.229 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.294 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.282 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.473 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.590 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.622 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.655 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.407 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.273 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.202 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.197 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.608 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.749 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.310 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.365 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.423 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.711 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.336 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.536 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.297 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.645 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.612 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.636 |
MOD_SUMO_rev_2 | 111 | 121 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 360 | 370 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_1 | 35 | 40 | PF01217 | 0.281 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.229 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.270 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.243 |
TRG_ER_diArg_1 | 462 | 464 | PF00400 | 0.634 |
TRG_NLS_MonoExtC_3 | 259 | 265 | PF00514 | 0.360 |
TRG_NLS_MonoExtN_4 | 257 | 264 | PF00514 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.724 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7R8 | Leptomonas seymouri | 63% | 94% |
A0A1X0NUC1 | Trypanosomatidae | 44% | 87% |
A0A3S7WTG9 | Leishmania donovani | 100% | 100% |
A0A422NRC0 | Trypanosoma rangeli | 41% | 97% |
A4H848 | Leishmania braziliensis | 67% | 99% |
C9ZXX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AQ75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4QFA8 | Leishmania major | 90% | 100% |
V5BK24 | Trypanosoma cruzi | 41% | 97% |