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: 5 |
NetGPI | no | yes: 0, no: 5 |
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: E9ALU0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
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 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0106310 | protein serine kinase activity | 4 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.389 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.687 |
CLV_PCSK_PC7_1 | 36 | 42 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.400 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.517 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.505 |
DOC_CYCLIN_RxL_1 | 34 | 47 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 545 | 551 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 315 | 325 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 386 | 395 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.505 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.231 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.636 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 436 | 440 | PF00244 | 0.214 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 570 | 580 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 59 | 68 | PF00244 | 0.480 |
LIG_Actin_WH2_2 | 245 | 260 | PF00022 | 0.484 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.505 |
LIG_CtBP_PxDLS_1 | 515 | 519 | PF00389 | 0.505 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.541 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.643 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.634 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.505 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.373 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.330 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.505 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.241 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.408 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 405 | 411 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 462 | 468 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 132 | 141 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.349 |
LIG_NRP_CendR_1 | 584 | 586 | PF00754 | 0.514 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.505 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 509 | 512 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.505 |
LIG_SH3_2 | 415 | 420 | PF14604 | 0.330 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.640 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.683 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.505 |
LIG_Sin3_3 | 110 | 117 | PF02671 | 0.490 |
LIG_SUMO_SIM_anti_2 | 333 | 340 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 274 | 280 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 546 | 552 | PF11976 | 0.501 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.214 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.214 |
LIG_UBA3_1 | 286 | 291 | PF00899 | 0.262 |
LIG_UBA3_1 | 558 | 565 | PF00899 | 0.505 |
LIG_WW_1 | 497 | 500 | PF00397 | 0.505 |
MOD_CDC14_SPxK_1 | 22 | 25 | PF00782 | 0.808 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.808 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 244 | 251 | PF00069 | 0.549 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.680 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.783 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.711 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.602 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.497 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.522 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.801 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.565 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.505 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.505 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.505 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.491 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.432 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.560 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.441 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.214 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.500 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.505 |
MOD_DYRK1A_RPxSP_1 | 197 | 201 | PF00069 | 0.507 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.639 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.765 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.698 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.610 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.582 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.693 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.759 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.670 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.580 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.505 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.505 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.505 |
MOD_GlcNHglycan | 475 | 479 | PF01048 | 0.439 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.350 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.341 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.505 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.531 |
MOD_GlcNHglycan | 80 | 85 | PF01048 | 0.623 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.626 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.719 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.471 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.633 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.784 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.578 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.560 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.740 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.589 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.589 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.505 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.505 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.310 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.482 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.463 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.491 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.220 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.609 |
MOD_LATS_1 | 180 | 186 | PF00433 | 0.725 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.505 |
MOD_N-GLC_2 | 540 | 542 | PF02516 | 0.330 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.752 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.747 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.523 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.805 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.505 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.359 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.280 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.321 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.493 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.510 |
MOD_NEK2_2 | 435 | 440 | PF00069 | 0.214 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.552 |
MOD_OFUCOSY | 60 | 65 | PF10250 | 0.476 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.427 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.770 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.495 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.538 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.505 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.505 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.373 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.214 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.466 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.505 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.521 |
MOD_Plk_2-3 | 446 | 452 | PF00069 | 0.214 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.799 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.359 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.344 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.344 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.382 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.693 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.652 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.806 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.729 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.772 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.505 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.505 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.427 |
MOD_SUMO_for_1 | 388 | 391 | PF00179 | 0.505 |
TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.214 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.789 |
TRG_DiLeu_BaLyEn_6 | 65 | 70 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.783 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.790 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.760 |
TRG_Pf-PMV_PEXEL_1 | 301 | 306 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J842 | Bodo saltans | 23% | 100% |
A0A1X0P0R3 | Trypanosomatidae | 26% | 97% |
A0A3Q8INQ4 | Leishmania donovani | 27% | 100% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A0A3S7X2F1 | Leishmania donovani | 86% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4HA97 | Leishmania braziliensis | 24% | 100% |
A4HED7 | Leishmania braziliensis | 29% | 100% |
A4HHE4 | Leishmania braziliensis | 72% | 100% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4HW76 | Leishmania infantum | 22% | 73% |
A4I1T4 | Leishmania infantum | 27% | 100% |
A5GFW1 | Sus scrofa | 31% | 100% |
E9ADZ1 | Leishmania major | 84% | 100% |
E9AHI7 | Leishmania infantum | 86% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9ASL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
P25341 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 81% |
P83099 | Drosophila melanogaster | 25% | 87% |
Q4Q9K2 | Leishmania major | 27% | 100% |
Q4QAV8 | Leishmania major | 28% | 100% |
Q4QJJ0 | Leishmania major | 27% | 100% |
Q8LPD9 | Chlamydomonas reinhardtii | 26% | 78% |
V5B639 | Trypanosoma cruzi | 27% | 84% |