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: A0A3Q8INL6
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 | 0.447 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.498 |
DOC_ANK_TNKS_1 | 316 | 323 | PF00023 | 0.562 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.445 |
DOC_CYCLIN_RxL_1 | 472 | 482 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 431 | 440 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 511 | 519 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.368 |
DOC_MAPK_NFAT4_5 | 257 | 265 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.431 |
DOC_PP1_RVXF_1 | 473 | 480 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.399 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.588 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.463 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.162 |
LIG_14-3-3_CanoR_1 | 512 | 517 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.637 |
LIG_APCC_ABBA_1 | 165 | 170 | PF00400 | 0.454 |
LIG_APCC_ABBA_1 | 438 | 443 | PF00400 | 0.445 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.617 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.493 |
LIG_CSL_BTD_1 | 249 | 252 | PF09270 | 0.398 |
LIG_CtBP_PxDLS_1 | 90 | 94 | PF00389 | 0.362 |
LIG_DLG_GKlike_1 | 271 | 278 | PF00625 | 0.461 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.597 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.399 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.538 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.540 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.398 |
LIG_Integrin_RGD_1 | 224 | 226 | PF01839 | 0.550 |
LIG_LIR_Apic_2 | 166 | 171 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 314 | 323 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.515 |
LIG_PAM2_1 | 378 | 390 | PF00658 | 0.657 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.483 |
LIG_PTAP_UEV_1 | 379 | 384 | PF05743 | 0.716 |
LIG_PTB_Apo_2 | 58 | 65 | PF02174 | 0.301 |
LIG_PTB_Phospho_1 | 58 | 64 | PF10480 | 0.288 |
LIG_RPA_C_Fungi | 266 | 278 | PF08784 | 0.462 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.416 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.318 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 141 | 145 | PF00017 | 0.477 |
LIG_SH2_SRC | 427 | 430 | PF00017 | 0.354 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 521 | 525 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.598 |
LIG_SH3_1 | 377 | 383 | PF00018 | 0.625 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.528 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.564 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.754 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 256 | 263 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 163 | 170 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 259 | 266 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.372 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.410 |
LIG_WW_1 | 6 | 9 | PF00397 | 0.439 |
MOD_CDK_SPxxK_3 | 370 | 377 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 479 | 486 | PF00069 | 0.412 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.462 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.654 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.439 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.631 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.477 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.779 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.396 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.556 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.525 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.526 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.559 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.593 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.445 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.398 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.434 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.597 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.719 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.448 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.499 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.591 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.625 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.575 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.395 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.373 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.379 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.659 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.476 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.636 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.392 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.575 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.633 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.497 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.680 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.549 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.693 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.214 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.530 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.349 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.597 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.410 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.383 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.518 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.429 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.362 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.318 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.431 |
MOD_PK_1 | 512 | 518 | PF00069 | 0.295 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.401 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.371 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.459 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.540 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.399 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.681 |
MOD_PKB_1 | 222 | 230 | PF00069 | 0.451 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.678 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.356 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.531 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.371 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.559 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.427 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.555 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.410 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.295 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.463 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.462 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.578 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.457 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P722 | Leptomonas seymouri | 51% | 100% |
A0A1X0P849 | Trypanosomatidae | 34% | 100% |
A4HP31 | Leishmania braziliensis | 75% | 100% |
A4IDD8 | Leishmania infantum | 99% | 100% |
D0A314 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AST9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1Q7 | Leishmania major | 91% | 100% |