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) | 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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4I1A1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.609 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.438 |
CLV_PCSK_FUR_1 | 105 | 109 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.580 |
DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 170 | 174 | PF00917 | 0.483 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.439 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.501 |
DOC_ANK_TNKS_1 | 107 | 114 | PF00023 | 0.517 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.348 |
DOC_PP1_RVXF_1 | 113 | 119 | PF00149 | 0.311 |
DOC_PP2B_LxvP_1 | 179 | 182 | PF13499 | 0.434 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.468 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 4 | 11 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 20 | 35 | PF00022 | 0.352 |
LIG_BIR_III_2 | 344 | 348 | PF00653 | 0.528 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.473 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.512 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.340 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.495 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.463 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.594 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.606 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.740 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.755 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.348 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.447 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.642 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.463 |
LIG_GBD_Chelix_1 | 145 | 153 | PF00786 | 0.488 |
LIG_LIR_Apic_2 | 394 | 398 | PF02991 | 0.629 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 251 | 258 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 38 | 47 | PF02991 | 0.455 |
LIG_LIR_LC3C_4 | 221 | 225 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 370 | 374 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.448 |
LIG_MYND_1 | 386 | 390 | PF01753 | 0.642 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.499 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.316 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.552 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.385 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.446 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.626 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.406 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.461 |
LIG_WRC_WIRS_1 | 250 | 255 | PF05994 | 0.371 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.284 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.717 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.505 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.386 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.694 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.723 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.490 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.419 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.452 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.452 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.402 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.519 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.410 |
MOD_GlcNHglycan | 206 | 211 | PF01048 | 0.372 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.342 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.701 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.405 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.517 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.701 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.507 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.381 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.423 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.521 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.425 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.654 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.542 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.588 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.707 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.297 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.405 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.521 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.434 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.379 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.549 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.547 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.457 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.677 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.512 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.776 |
MOD_PK_1 | 271 | 277 | PF00069 | 0.418 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.395 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.390 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.421 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.608 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.466 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.482 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.511 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.442 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.392 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.323 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.342 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.603 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.671 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5X9 | Leptomonas seymouri | 53% | 98% |
A0A0S4IKU6 | Bodo saltans | 24% | 100% |
A0A1X0P4Q1 | Trypanosomatidae | 30% | 100% |
A0A3S5IS63 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WZ17 | Leishmania donovani | 100% | 100% |
A4HEF8 | Leishmania braziliensis | 75% | 100% |
D0A5J3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AXD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QA35 | Leishmania major | 89% | 100% |
V5B7R1 | Trypanosoma cruzi | 29% | 100% |