A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
Protein kinase, Ser/Thr kinase
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: 16 |
NetGPI | no | yes: 0, no: 16 |
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 | 2 |
GO:0016020 | membrane | 2 | 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: E9AGR6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 17 |
GO:0006793 | phosphorus metabolic process | 3 | 17 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 17 |
GO:0006807 | nitrogen compound metabolic process | 2 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0016310 | phosphorylation | 5 | 17 |
GO:0019538 | protein metabolic process | 3 | 17 |
GO:0036211 | protein modification process | 4 | 17 |
GO:0043170 | macromolecule metabolic process | 3 | 17 |
GO:0043412 | macromolecule modification | 4 | 17 |
GO:0044237 | cellular metabolic process | 2 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 17 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 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 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004672 | protein kinase activity | 3 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016301 | kinase activity | 4 | 17 |
GO:0016740 | transferase activity | 2 | 17 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 17 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0042802 | identical protein binding | 3 | 1 |
GO:0042803 | protein homodimerization activity | 4 | 1 |
GO:0046983 | protein dimerization activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.200 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.203 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.218 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.218 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.220 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.189 |
CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.189 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.191 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.648 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.231 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.278 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.292 |
DOC_CYCLIN_yCln2_LP_2 | 323 | 329 | PF00134 | 0.307 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.267 |
DOC_MAPK_gen_1 | 568 | 576 | PF00069 | 0.186 |
DOC_MAPK_JIP1_4 | 165 | 171 | PF00069 | 0.229 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.242 |
DOC_PP4_FxxP_1 | 612 | 615 | PF00568 | 0.186 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.198 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.523 |
DOC_USP7_UBL2_3 | 311 | 315 | PF12436 | 0.227 |
DOC_USP7_UBL2_3 | 56 | 60 | PF12436 | 0.258 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.219 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.147 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.234 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 220 | 230 | PF00244 | 0.224 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.189 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 413 | 420 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 425 | 429 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 451 | 456 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 503 | 513 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 623 | 630 | PF00244 | 0.195 |
LIG_Actin_WH2_2 | 75 | 92 | PF00022 | 0.246 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.187 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.186 |
LIG_BRCT_BRCA1_1 | 578 | 582 | PF00533 | 0.278 |
LIG_Clathr_ClatBox_1 | 112 | 116 | PF01394 | 0.186 |
LIG_Dynein_DLC8_1 | 239 | 245 | PF01221 | 0.200 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.223 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.219 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.500 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.672 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.607 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.328 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.186 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.197 |
LIG_LIR_Apic_2 | 229 | 235 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 144 | 152 | PF02991 | 0.186 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.199 |
LIG_LIR_Gen_1 | 261 | 270 | PF02991 | 0.213 |
LIG_LIR_Gen_1 | 317 | 328 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.189 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.199 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 261 | 265 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.249 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.193 |
LIG_Pex14_2 | 238 | 242 | PF04695 | 0.186 |
LIG_REV1ctd_RIR_1 | 112 | 121 | PF16727 | 0.333 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.186 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.218 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.364 |
LIG_SH2_PTP2 | 262 | 265 | PF00017 | 0.283 |
LIG_SH2_PTP2 | 46 | 49 | PF00017 | 0.333 |
LIG_SH2_SRC | 145 | 148 | PF00017 | 0.190 |
LIG_SH2_SRC | 46 | 49 | PF00017 | 0.200 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.180 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.200 |
LIG_SH2_STAT3 | 143 | 146 | PF00017 | 0.186 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.216 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.106 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.186 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.158 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.305 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.333 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.196 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.433 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 85 | 90 | PF11976 | 0.216 |
LIG_SUMO_SIM_par_1 | 199 | 204 | PF11976 | 0.284 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.666 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.283 |
LIG_UBA3_1 | 67 | 72 | PF00899 | 0.218 |
LIG_WRC_WIRS_1 | 98 | 103 | PF05994 | 0.200 |
MOD_CDC14_SPxK_1 | 428 | 431 | PF00782 | 0.499 |
MOD_CDK_SPK_2 | 193 | 198 | PF00069 | 0.179 |
MOD_CDK_SPK_2 | 226 | 231 | PF00069 | 0.186 |
MOD_CDK_SPxK_1 | 425 | 431 | PF00069 | 0.498 |
MOD_CDK_SPxK_1 | 472 | 478 | PF00069 | 0.519 |
MOD_CDK_SPxK_1 | 480 | 486 | PF00069 | 0.519 |
MOD_CDK_SPxK_1 | 509 | 515 | PF00069 | 0.538 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.466 |
MOD_CDK_SPxxK_3 | 286 | 293 | PF00069 | 0.340 |
MOD_CDK_SPxxK_3 | 457 | 464 | PF00069 | 0.524 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.333 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.306 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.390 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.479 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.582 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.621 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.524 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.577 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.481 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.264 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.197 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.200 |
MOD_DYRK1A_RPxSP_1 | 404 | 408 | PF00069 | 0.514 |
MOD_DYRK1A_RPxSP_1 | 425 | 429 | PF00069 | 0.552 |
MOD_DYRK1A_RPxSP_1 | 486 | 490 | PF00069 | 0.506 |
MOD_DYRK1A_RPxSP_1 | 515 | 519 | PF00069 | 0.524 |
MOD_DYRK1A_RPxSP_1 | 526 | 530 | PF00069 | 0.525 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.341 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.240 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.319 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.444 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.411 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.619 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.594 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.505 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.482 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.517 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.454 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.604 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.624 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.503 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.508 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.255 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.225 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.199 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.238 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.605 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.565 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.514 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.697 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.457 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.556 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.502 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.519 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.589 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.186 |
MOD_LATS_1 | 435 | 441 | PF00433 | 0.532 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.333 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.717 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.278 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.327 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.344 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.240 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.203 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.323 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.482 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.665 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.528 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.644 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.316 |
MOD_NEK2_2 | 420 | 425 | PF00069 | 0.613 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.238 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.445 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.186 |
MOD_PKA_1 | 451 | 457 | PF00069 | 0.575 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.443 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.416 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.633 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.538 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.541 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.539 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.551 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.186 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.362 |
MOD_Plk_2-3 | 601 | 607 | PF00069 | 0.186 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.237 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.310 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.315 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.388 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.383 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.199 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.197 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.317 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.219 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.326 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.147 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.234 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.388 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.230 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.586 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.513 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.521 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.519 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.519 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.520 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.465 |
MOD_SUMO_for_1 | 164 | 167 | PF00179 | 0.267 |
MOD_SUMO_for_1 | 82 | 85 | PF00179 | 0.186 |
MOD_SUMO_rev_2 | 131 | 140 | PF00179 | 0.213 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.186 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.200 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.200 |
TRG_DiLeu_BaEn_4 | 137 | 143 | PF01217 | 0.278 |
TRG_DiLeu_BaEn_4 | 361 | 367 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 212 | 217 | PF01217 | 0.218 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.186 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.493 |
TRG_ER_diLys_1 | 628 | 631 | PF00400 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M7 | Leptomonas seymouri | 83% | 98% |
A0A0S4IX25 | Bodo saltans | 45% | 97% |
A0A0S4J320 | Bodo saltans | 24% | 100% |
A0A0S4JVD7 | Bodo saltans | 25% | 100% |
A0A1X0P6L8 | Trypanosomatidae | 67% | 100% |
A0A3R7LU08 | Trypanosoma rangeli | 65% | 100% |
A0A3S5H5G0 | Leishmania donovani | 28% | 100% |
A0A3S7WV74 | Leishmania donovani | 100% | 100% |
A0A3S7WY10 | Leishmania donovani | 26% | 100% |
A0A3S7X8Z8 | Leishmania donovani | 26% | 100% |
A0A422P2B2 | Trypanosoma rangeli | 25% | 100% |
A4H459 | Leishmania braziliensis | 29% | 100% |
A4H4S9 | Leishmania braziliensis | 27% | 100% |
A4H9X1 | Leishmania braziliensis | 92% | 100% |
A4HCD7 | Leishmania braziliensis | 29% | 100% |
A4HSE2 | Leishmania infantum | 28% | 100% |
A4IB02 | Leishmania infantum | 26% | 100% |
D0A0D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 99% |
E9AET0 | Leishmania major | 25% | 100% |
E9AH34 | Leishmania infantum | 26% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9ARW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 99% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q42396 | Arabidopsis thaliana | 28% | 100% |
Q4QAV8 | Leishmania major | 26% | 100% |
Q4QDK7 | Leishmania major | 98% | 100% |
Q4QIV8 | Leishmania major | 25% | 100% |
Q4QJJ0 | Leishmania major | 27% | 100% |
Q7TNJ7 | Rattus norvegicus | 28% | 100% |
Q852Q2 | Oryza sativa subsp. japonica | 26% | 100% |
V5DTI3 | Trypanosoma cruzi | 65% | 100% |