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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I616
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.830 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 114 | 118 | PF03568 | 0.511 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.515 |
DEG_COP1_1 | 71 | 79 | PF00400 | 0.567 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.584 |
DOC_CDC14_PxL_1 | 73 | 81 | PF14671 | 0.565 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.583 |
DOC_CKS1_1 | 250 | 255 | PF01111 | 0.703 |
DOC_CKS1_1 | 312 | 317 | PF01111 | 0.679 |
DOC_CYCLIN_yCln2_LP_2 | 290 | 296 | PF00134 | 0.593 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.584 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.496 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.767 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 199 | 208 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.515 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.514 |
LIG_CtBP_PxDLS_1 | 26 | 30 | PF00389 | 0.658 |
LIG_deltaCOP1_diTrp_1 | 169 | 176 | PF00928 | 0.464 |
LIG_EVH1_1 | 242 | 246 | PF00568 | 0.723 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.512 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.457 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.560 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.694 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.750 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.575 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.525 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.475 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.724 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 139 | 147 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 157 | 162 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.509 |
LIG_MYND_1 | 235 | 239 | PF01753 | 0.574 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.482 |
LIG_REV1ctd_RIR_1 | 140 | 150 | PF16727 | 0.451 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.700 |
LIG_SH2_CRK | 354 | 358 | PF00017 | 0.740 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.512 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.780 |
LIG_SH2_SRC | 336 | 339 | PF00017 | 0.731 |
LIG_SH2_SRC | 354 | 357 | PF00017 | 0.734 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.508 |
LIG_SH3_1 | 74 | 80 | PF00018 | 0.568 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.532 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.555 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.560 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.577 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.616 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.748 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.735 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.685 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.661 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.568 |
LIG_SUMO_SIM_par_1 | 339 | 348 | PF11976 | 0.678 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.481 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.586 |
LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.570 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.461 |
MOD_CDC14_SPxK_1 | 153 | 156 | PF00782 | 0.568 |
MOD_CDK_SPxK_1 | 150 | 156 | PF00069 | 0.548 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.420 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.730 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.636 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.635 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.514 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.488 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.555 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.551 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.497 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.471 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.578 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.622 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.506 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.521 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.602 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.805 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.768 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.738 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.740 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.364 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.553 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.553 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.535 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.520 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.462 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.531 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.637 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.699 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.504 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.518 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.504 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.445 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.621 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.502 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.518 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.455 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.480 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.548 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.680 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.583 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.693 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.707 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.543 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.679 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.769 |
MOD_SUMO_rev_2 | 68 | 76 | PF00179 | 0.552 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.505 |
TRG_NES_CRM1_1 | 85 | 99 | PF08389 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P436 | Leptomonas seymouri | 62% | 96% |
A0A3Q8IG34 | Leishmania donovani | 99% | 100% |
A4HIS0 | Leishmania braziliensis | 77% | 100% |
E9B1A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4Q6V7 | Leishmania major | 89% | 99% |
V5BSD6 | Trypanosoma cruzi | 53% | 90% |