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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S7WZA6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.795 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.314 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.772 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.730 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.345 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.445 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.462 |
DOC_CDC14_PxL_1 | 433 | 441 | PF14671 | 0.721 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.462 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.321 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 405 | 414 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.314 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.248 |
DOC_USP7_UBL2_3 | 278 | 282 | PF12436 | 0.651 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.345 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.132 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.237 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 365 | 372 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 481 | 487 | PF00244 | 0.737 |
LIG_Actin_WH2_2 | 349 | 367 | PF00022 | 0.377 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.675 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.336 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.288 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.688 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.403 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.720 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.304 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.307 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.377 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.744 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.731 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.666 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 352 | 360 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 525 | 535 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 568 | 576 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.618 |
LIG_MYND_1 | 375 | 379 | PF01753 | 0.457 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.676 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.629 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.664 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.648 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.211 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.337 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.420 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.321 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.322 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.681 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.655 |
LIG_SH3_4 | 396 | 403 | PF00018 | 0.665 |
LIG_TYR_ITSM | 303 | 310 | PF00017 | 0.377 |
LIG_WRC_WIRS_1 | 350 | 355 | PF05994 | 0.406 |
LIG_WW_1 | 265 | 268 | PF00397 | 0.712 |
MOD_CDC14_SPxK_1 | 478 | 481 | PF00782 | 0.711 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.365 |
MOD_CDK_SPK_2 | 475 | 480 | PF00069 | 0.572 |
MOD_CDK_SPxK_1 | 159 | 165 | PF00069 | 0.287 |
MOD_CDK_SPxK_1 | 475 | 481 | PF00069 | 0.711 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.401 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.365 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.551 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.669 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.757 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.674 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.642 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.685 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.529 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.420 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.720 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.314 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.345 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.771 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.670 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.729 |
MOD_Cter_Amidation | 403 | 406 | PF01082 | 0.564 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.692 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.726 |
MOD_GlcNHglycan | 259 | 263 | PF01048 | 0.699 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.340 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.376 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.389 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.710 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.672 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.701 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.748 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.734 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.644 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.567 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.653 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.676 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.411 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.377 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.763 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.367 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.264 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.675 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.722 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.714 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.705 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.699 |
MOD_N-GLC_2 | 229 | 231 | PF02516 | 0.542 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.415 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.763 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.602 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.383 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.744 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.721 |
MOD_NEK2_2 | 428 | 433 | PF00069 | 0.620 |
MOD_NEK2_2 | 482 | 487 | PF00069 | 0.644 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.785 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.333 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.657 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.734 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.678 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.384 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.648 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.625 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.321 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.406 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.669 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.401 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.132 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.445 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.237 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.716 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.339 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.660 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.711 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.723 |
MOD_SUMO_rev_2 | 389 | 397 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_2 | 348 | 354 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_2 | 567 | 573 | PF01217 | 0.673 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.655 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.797 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.648 |
TRG_NES_CRM1_1 | 118 | 133 | PF08389 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W2 | Leptomonas seymouri | 54% | 96% |
A0A0S4JI27 | Bodo saltans | 24% | 80% |
A0A1X0NYS1 | Trypanosomatidae | 41% | 100% |
A0A422P4L8 | Trypanosoma rangeli | 46% | 100% |
A4HEA1 | Leishmania braziliensis | 78% | 98% |
A4I1P7 | Leishmania infantum | 99% | 100% |
A4K2S1 | Lemur catta | 27% | 100% |
C9ZK98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AXT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P22216 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 70% |
Q4Q9P0 | Leishmania major | 93% | 100% |
Q5ZJK4 | Gallus gallus | 26% | 100% |
Q99078 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 100% |
Q9JI11 | Mus musculus | 27% | 100% |