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: 10 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHW0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.490 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.363 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.325 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 464 | 466 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.344 |
DEG_Kelch_Keap1_1 | 511 | 516 | PF01344 | 0.430 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.443 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.529 |
DOC_PP4_FxxP_1 | 10 | 13 | PF00568 | 0.584 |
DOC_PP4_FxxP_1 | 532 | 535 | PF00568 | 0.363 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.740 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 265 | 273 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 422 | 431 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.805 |
LIG_APCC_ABBA_1 | 406 | 411 | PF00400 | 0.425 |
LIG_BIR_III_4 | 420 | 424 | PF00653 | 0.412 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.558 |
LIG_Clathr_ClatBox_1 | 190 | 194 | PF01394 | 0.309 |
LIG_deltaCOP1_diTrp_1 | 259 | 266 | PF00928 | 0.430 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.605 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.519 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.447 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.583 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.460 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.464 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.504 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.485 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.523 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.620 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.602 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.347 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.320 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.324 |
LIG_Integrin_isoDGR_2 | 504 | 506 | PF01839 | 0.441 |
LIG_LIR_Apic_2 | 169 | 175 | PF02991 | 0.437 |
LIG_LIR_Apic_2 | 530 | 535 | PF02991 | 0.356 |
LIG_LIR_Apic_2 | 7 | 13 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.459 |
LIG_PCNA_PIPBox_1 | 244 | 253 | PF02747 | 0.450 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.275 |
LIG_SH3_1 | 172 | 178 | PF00018 | 0.511 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.473 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.280 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.457 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.652 |
LIG_SH3_4 | 428 | 435 | PF00018 | 0.393 |
LIG_SUMO_SIM_par_1 | 453 | 459 | PF11976 | 0.388 |
LIG_UBA3_1 | 517 | 522 | PF00899 | 0.331 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.446 |
MOD_CDK_SPxxK_3 | 131 | 138 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 146 | 153 | PF00069 | 0.618 |
MOD_CDK_SPxxK_3 | 206 | 213 | PF00069 | 0.539 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.808 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.524 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.535 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.530 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.795 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.701 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.560 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.326 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.446 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.435 |
MOD_DYRK1A_RPxSP_1 | 445 | 449 | PF00069 | 0.350 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.582 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.714 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.576 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.212 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.238 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.380 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.158 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.599 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.424 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.339 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.588 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.614 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.536 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.384 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.308 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.603 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.432 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.471 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.543 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.722 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.727 |
MOD_N-GLC_2 | 311 | 313 | PF02516 | 0.262 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.618 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.541 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.441 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.486 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.437 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.466 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.257 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.645 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.762 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.430 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.430 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.495 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.616 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.516 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.778 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.817 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.796 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.822 |
MOD_PKB_1 | 55 | 63 | PF00069 | 0.536 |
MOD_PKB_1 | 76 | 84 | PF00069 | 0.540 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.430 |
MOD_Plk_2-3 | 240 | 246 | PF00069 | 0.356 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.535 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.438 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.356 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.451 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.387 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.735 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.586 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.620 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.584 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.448 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.362 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.342 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.762 |
MOD_SUMO_rev_2 | 240 | 250 | PF00179 | 0.319 |
MOD_SUMO_rev_2 | 274 | 281 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 516 | 523 | PF00179 | 0.330 |
TRG_DiLeu_BaEn_1 | 513 | 518 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 503 | 508 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 506 | 511 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMQ0 | Leptomonas seymouri | 69% | 100% |
A0A1X0P1V8 | Trypanosomatidae | 56% | 100% |
A0A3R7MF36 | Trypanosoma rangeli | 51% | 100% |
A4H666 | Leishmania braziliensis | 24% | 100% |
A4HI91 | Leishmania braziliensis | 80% | 100% |
A4I5H1 | Leishmania infantum | 99% | 100% |
C9ZQV5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AN88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B0R9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q7G4 | Leishmania major | 93% | 100% |
V5BYY0 | Trypanosoma cruzi | 51% | 100% |