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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IBT7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.456 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.562 |
DEG_SPOP_SBC_1 | 376 | 380 | PF00917 | 0.660 |
DOC_CKS1_1 | 257 | 262 | PF01111 | 0.620 |
DOC_CYCLIN_RxL_1 | 189 | 198 | PF00134 | 0.465 |
DOC_CYCLIN_yCln2_LP_2 | 415 | 418 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 68 | 74 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 227 | 236 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 395 | 403 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 342 | 349 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.556 |
DOC_PP2B_PxIxI_1 | 120 | 126 | PF00149 | 0.404 |
DOC_PP4_FxxP_1 | 14 | 17 | PF00568 | 0.366 |
DOC_PP4_FxxP_1 | 403 | 406 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 83 | 86 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.458 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 395 | 405 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 98 | 102 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 143 | 158 | PF00022 | 0.458 |
LIG_Actin_WH2_2 | 285 | 303 | PF00022 | 0.508 |
LIG_EVH1_2 | 407 | 411 | PF00568 | 0.393 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.430 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.548 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.604 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.578 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.523 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.444 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.505 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.383 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.598 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.505 |
LIG_FXI_DFP_1 | 6 | 10 | PF00024 | 0.322 |
LIG_LIR_Apic_2 | 12 | 17 | PF02991 | 0.355 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 205 | 213 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 294 | 305 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.479 |
LIG_PDZ_Class_1 | 448 | 453 | PF00595 | 0.505 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.449 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.447 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.429 |
LIG_SH3_2 | 71 | 76 | PF14604 | 0.464 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.493 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.458 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.510 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.313 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.467 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.445 |
LIG_TRAF2_1 | 439 | 442 | PF00917 | 0.501 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.528 |
LIG_UBA3_1 | 87 | 96 | PF00899 | 0.366 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.419 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.632 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.616 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.572 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.466 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.500 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.614 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.495 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.576 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.475 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.527 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.597 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.602 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.475 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.441 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.399 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.752 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.748 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.576 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.431 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.610 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.681 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.552 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.511 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.345 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.451 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.459 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.597 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.598 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.436 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.338 |
MOD_PK_1 | 423 | 429 | PF00069 | 0.466 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.512 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.527 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.500 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.466 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.471 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.466 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.424 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.340 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.374 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.595 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.621 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.663 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.578 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.594 |
MOD_SUMO_rev_2 | 320 | 328 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 441 | 446 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_2 | 78 | 84 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_4 | 442 | 448 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2R2 | Leptomonas seymouri | 46% | 100% |
A4HCX8 | Leishmania braziliensis | 72% | 100% |
A4I0G1 | Leishmania infantum | 100% | 100% |
E9AWC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QB48 | Leishmania major | 94% | 100% |