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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AXT1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
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_NRD_NRD_1 | 427 | 429 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.569 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.292 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.355 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.276 |
DOC_CDC14_PxL_1 | 431 | 439 | PF14671 | 0.538 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.276 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.135 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.236 |
DOC_CYCLIN_RxL_1 | 394 | 404 | PF00134 | 0.459 |
DOC_CYCLIN_yClb3_PxF_3 | 395 | 403 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.280 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.236 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.259 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.616 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.258 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.135 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.235 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.278 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 537 | 547 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 347 | 365 | PF00022 | 0.292 |
LIG_APCC_ABBAyCdc20_2 | 34 | 40 | PF00400 | 0.152 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.532 |
LIG_Clathr_ClatBox_1 | 36 | 40 | PF01394 | 0.152 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.287 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.242 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.611 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.322 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.236 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.236 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.338 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.752 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.555 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.278 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.602 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.276 |
LIG_LIR_Apic_2 | 544 | 550 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 350 | 358 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 566 | 574 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 566 | 570 | PF02991 | 0.526 |
LIG_MYND_1 | 373 | 377 | PF01753 | 0.438 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.537 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.568 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.428 |
LIG_SH2_CRK | 547 | 551 | PF00017 | 0.451 |
LIG_SH2_GRB2like | 271 | 274 | PF00017 | 0.582 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.309 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.359 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.278 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.289 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.681 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.618 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.568 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.512 |
LIG_TYR_ITSM | 301 | 308 | PF00017 | 0.292 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.329 |
LIG_WW_1 | 263 | 266 | PF00397 | 0.650 |
LIG_WW_3 | 394 | 398 | PF00397 | 0.455 |
MOD_CDC14_SPxK_1 | 476 | 479 | PF00782 | 0.569 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.235 |
MOD_CDK_SPxK_1 | 159 | 165 | PF00069 | 0.202 |
MOD_CDK_SPxK_1 | 473 | 479 | PF00069 | 0.570 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.351 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.235 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.623 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.585 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.621 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.605 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.631 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.555 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.364 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.654 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.236 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.303 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.735 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.568 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.575 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.716 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.534 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.637 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.318 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.292 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.306 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.638 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.600 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.746 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.709 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.585 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.526 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.518 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.592 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.684 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.336 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.338 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.756 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.757 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.282 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.237 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.524 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.556 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.610 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.694 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.660 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.634 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.258 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.737 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.521 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.332 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.583 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.701 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.303 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.568 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.683 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.621 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.243 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.575 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.266 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.329 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.543 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.351 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.135 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.235 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.278 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.681 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.254 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.589 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.575 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.693 |
TRG_DiLeu_BaEn_2 | 346 | 352 | PF01217 | 0.276 |
TRG_DiLeu_BaEn_2 | 565 | 571 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 529 | 532 | PF00400 | 0.528 |
TRG_NES_CRM1_1 | 118 | 133 | PF08389 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W2 | Leptomonas seymouri | 55% | 96% |
A0A1X0NYS1 | Trypanosomatidae | 41% | 100% |
A0A3S7WZA6 | Leishmania donovani | 90% | 100% |
A0A422P4L8 | Trypanosoma rangeli | 44% | 100% |
A4HEA1 | Leishmania braziliensis | 79% | 99% |
A4I1P7 | Leishmania infantum | 89% | 99% |
C9ZK98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AKZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q1PFB9 | Arabidopsis thaliana | 24% | 100% |
Q4Q9P0 | Leishmania major | 90% | 100% |