Uncharacterized Protein, Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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 |
Related structures:
AlphaFold database: E9AGI4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.706 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.517 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.497 |
DEG_SCF_FBW7_2 | 375 | 382 | PF00400 | 0.591 |
DOC_CKS1_1 | 183 | 188 | PF01111 | 0.540 |
DOC_CKS1_1 | 423 | 428 | PF01111 | 0.595 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.603 |
DOC_CYCLIN_RxL_1 | 59 | 67 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.607 |
DOC_MAPK_gen_1 | 365 | 372 | PF00069 | 0.683 |
DOC_MAPK_gen_1 | 50 | 59 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.499 |
DOC_PP2B_LxvP_1 | 281 | 284 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.730 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 314 | 318 | PF12436 | 0.650 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.666 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 277 | 282 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 365 | 372 | PF00244 | 0.661 |
LIG_Actin_WH2_2 | 324 | 339 | PF00022 | 0.548 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.508 |
LIG_deltaCOP1_diTrp_1 | 117 | 127 | PF00928 | 0.462 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.610 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.589 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.543 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.528 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.599 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.580 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.483 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.677 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.477 |
LIG_PDZ_Class_3 | 428 | 433 | PF00595 | 0.595 |
LIG_Pex14_1 | 123 | 127 | PF04695 | 0.476 |
LIG_REV1ctd_RIR_1 | 207 | 216 | PF16727 | 0.605 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.677 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.588 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.600 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.607 |
LIG_SH3_5 | 186 | 190 | PF00018 | 0.505 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 241 | 250 | PF11976 | 0.603 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.624 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.752 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.538 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.725 |
MOD_CDK_SPK_2 | 422 | 427 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 375 | 381 | PF00069 | 0.703 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.709 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.433 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.724 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.653 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.663 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.563 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.457 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.596 |
MOD_CMANNOS | 120 | 123 | PF00535 | 0.466 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.477 |
MOD_GlcNHglycan | 252 | 257 | PF01048 | 0.695 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.567 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.654 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.620 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.496 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.671 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.511 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.623 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.564 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.601 |
MOD_N-GLC_2 | 8 | 10 | PF02516 | 0.499 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.676 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.550 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.644 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.666 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.611 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.514 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.616 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.697 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.606 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.626 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.494 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.609 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.493 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.492 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.678 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.583 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.582 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.490 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.703 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.596 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 98 | 101 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 42 | 52 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.667 |
TRG_DiLeu_BaEn_2 | 100 | 106 | PF01217 | 0.494 |
TRG_DiLeu_BaEn_4 | 141 | 147 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_4 | 356 | 362 | PF01217 | 0.654 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.668 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY24 | Leptomonas seymouri | 45% | 75% |
A0A3Q8I9I2 | Leishmania donovani | 100% | 77% |
A4H700 | Leishmania braziliensis | 51% | 100% |
E9AP20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4QGG9 | Leishmania major | 84% | 100% |