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: A4HC95
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: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 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 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:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.688 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.542 |
CLV_Separin_Metazoa | 416 | 420 | PF03568 | 0.299 |
DEG_Kelch_Keap1_1 | 271 | 276 | PF01344 | 0.533 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.624 |
DOC_CDC14_PxL_1 | 388 | 396 | PF14671 | 0.299 |
DOC_CYCLIN_yCln2_LP_2 | 262 | 268 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 345 | 354 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 387 | 396 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 490 | 499 | PF00069 | 0.774 |
DOC_MAPK_HePTP_8 | 384 | 396 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 387 | 396 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 493 | 501 | PF00069 | 0.756 |
DOC_PP1_RVXF_1 | 322 | 329 | PF00149 | 0.342 |
DOC_PP1_RVXF_1 | 330 | 337 | PF00149 | 0.263 |
DOC_PP2B_LxvP_1 | 442 | 445 | PF13499 | 0.362 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.655 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.352 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 102 | 110 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 469 | 474 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 490 | 499 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.629 |
LIG_Actin_WH2_2 | 406 | 421 | PF00022 | 0.299 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
LIG_deltaCOP1_diTrp_1 | 406 | 410 | PF00928 | 0.299 |
LIG_eIF4E_1 | 389 | 395 | PF01652 | 0.299 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.299 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.474 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.611 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.389 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.299 |
LIG_GSK3_LRP6_1 | 285 | 290 | PF00069 | 0.503 |
LIG_HCF-1_HBM_1 | 197 | 200 | PF13415 | 0.470 |
LIG_LIR_Apic_2 | 386 | 392 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 221 | 230 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 409 | 413 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.400 |
LIG_REV1ctd_RIR_1 | 242 | 250 | PF16727 | 0.359 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.438 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.590 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.502 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.629 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.393 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 89 | 95 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 60 | 67 | PF11976 | 0.373 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.362 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.620 |
LIG_UBA3_1 | 438 | 447 | PF00899 | 0.299 |
LIG_WRC_WIRS_1 | 407 | 412 | PF05994 | 0.299 |
MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.655 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.421 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.590 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.621 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.597 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.610 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.666 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.534 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.654 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.358 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.575 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.299 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.499 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.594 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.668 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.756 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.663 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.645 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.647 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.539 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.531 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.545 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.749 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.646 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.643 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.318 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.299 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.766 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.662 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.561 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.795 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.602 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.659 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.715 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.358 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.528 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.554 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.544 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.614 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.750 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.656 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.601 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.299 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.648 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.325 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.503 |
MOD_N-GLC_1 | 491 | 496 | PF02516 | 0.479 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.670 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.513 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.446 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.299 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.422 |
MOD_OFUCOSY | 296 | 302 | PF10250 | 0.498 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.591 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.552 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.495 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.604 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.647 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.686 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.309 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.436 |
MOD_PKB_1 | 474 | 482 | PF00069 | 0.489 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.325 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.446 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.299 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.419 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.752 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.498 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.679 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.714 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.460 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.587 |
TRG_DiLeu_BaEn_4 | 508 | 514 | PF01217 | 0.517 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 490 | 493 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU16 | Leptomonas seymouri | 53% | 91% |
A0A3Q8IC49 | Leishmania donovani | 77% | 77% |
E9AVN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 77% |
Q4QBU7 | Leishmania major | 76% | 100% |