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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AST9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0101030 | tRNA-guanine transglycosylation | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.503 |
CLV_Separin_Metazoa | 277 | 281 | PF03568 | 0.247 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.492 |
DOC_CYCLIN_RxL_1 | 472 | 482 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 431 | 440 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 511 | 519 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.410 |
DOC_MAPK_NFAT4_5 | 257 | 265 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.477 |
DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.393 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.463 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.438 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.424 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.681 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 512 | 517 | PF00244 | 0.390 |
LIG_APCC_ABBA_1 | 412 | 417 | PF00400 | 0.201 |
LIG_APCC_ABBA_1 | 438 | 443 | PF00400 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 408 | 412 | PF00533 | 0.648 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.513 |
LIG_CSL_BTD_1 | 249 | 252 | PF09270 | 0.490 |
LIG_CtBP_PxDLS_1 | 90 | 94 | PF00389 | 0.393 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.626 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.408 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.395 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.429 |
LIG_Integrin_RGD_1 | 224 | 226 | PF01839 | 0.594 |
LIG_LIR_Apic_2 | 208 | 213 | PF02991 | 0.266 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 273 | 281 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 314 | 320 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.277 |
LIG_PAM2_1 | 378 | 390 | PF00658 | 0.665 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.505 |
LIG_PTAP_UEV_1 | 182 | 187 | PF05743 | 0.422 |
LIG_PTAP_UEV_1 | 379 | 384 | PF05743 | 0.710 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.357 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.438 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.280 |
LIG_SH2_SRC | 427 | 430 | PF00017 | 0.391 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.585 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.509 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.430 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.694 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.477 |
LIG_SUMO_SIM_anti_2 | 256 | 263 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 259 | 266 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.386 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.438 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.201 |
LIG_UBA3_1 | 476 | 485 | PF00899 | 0.269 |
MOD_CDK_SPxK_1 | 479 | 485 | PF00069 | 0.201 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.485 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.627 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.457 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.602 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.442 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.536 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.559 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.354 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.560 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.492 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.429 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.456 |
MOD_Cter_Amidation | 509 | 512 | PF01082 | 0.201 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.586 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.333 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.546 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.711 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.494 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.549 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.530 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.650 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.534 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.415 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.656 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.650 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.562 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.650 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.516 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.664 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.548 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.369 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.630 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.457 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.421 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.533 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.453 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.455 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.350 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.371 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.402 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.461 |
MOD_PK_1 | 512 | 518 | PF00069 | 0.317 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.638 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.420 |
MOD_PKB_1 | 222 | 230 | PF00069 | 0.485 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.652 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.393 |
MOD_Plk_2-3 | 401 | 407 | PF00069 | 0.426 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.552 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.407 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.518 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.453 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.625 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.487 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.384 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.430 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.266 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.317 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.535 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.475 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P722 | Leptomonas seymouri | 51% | 100% |
A0A1X0P849 | Trypanosomatidae | 34% | 100% |
A0A3Q8INL6 | Leishmania donovani | 89% | 100% |
A4HP31 | Leishmania braziliensis | 74% | 100% |
A4IDD8 | Leishmania infantum | 89% | 100% |
D0A314 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4Q1Q7 | Leishmania major | 88% | 100% |