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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AGZ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.643 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.549 |
DEG_COP1_1 | 150 | 158 | PF00400 | 0.661 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.782 |
DOC_CKS1_1 | 246 | 251 | PF01111 | 0.660 |
DOC_CKS1_1 | 259 | 264 | PF01111 | 0.608 |
DOC_CYCLIN_RxL_1 | 207 | 217 | PF00134 | 0.643 |
DOC_CYCLIN_RxL_1 | 8 | 16 | PF00134 | 0.610 |
DOC_CYCLIN_yCln2_LP_2 | 259 | 265 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 284 | 290 | PF00134 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 349 | 355 | PF00134 | 0.621 |
DOC_MAPK_gen_1 | 343 | 351 | PF00069 | 0.642 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.832 |
DOC_PP2B_LxvP_1 | 349 | 352 | PF13499 | 0.615 |
DOC_PP2B_PxIxI_1 | 109 | 115 | PF00149 | 0.558 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.696 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.642 |
DOC_USP7_UBL2_3 | 98 | 102 | PF12436 | 0.717 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 160 | 168 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 46 | 54 | PF00244 | 0.680 |
LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.585 |
LIG_BIR_III_4 | 41 | 45 | PF00653 | 0.698 |
LIG_EH1_1 | 7 | 15 | PF00400 | 0.687 |
LIG_eIF4E_1 | 73 | 79 | PF01652 | 0.730 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.678 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.630 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.652 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.645 |
LIG_GBD_Chelix_1 | 381 | 389 | PF00786 | 0.654 |
LIG_LIR_Apic_2 | 48 | 53 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.485 |
LIG_MYND_1 | 137 | 141 | PF01753 | 0.766 |
LIG_NRP_CendR_1 | 387 | 390 | PF00754 | 0.623 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.623 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.707 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 111 | 114 | PF00017 | 0.530 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.713 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.649 |
LIG_SUMO_SIM_anti_2 | 261 | 268 | PF11976 | 0.583 |
LIG_SUMO_SIM_anti_2 | 318 | 323 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 261 | 268 | PF11976 | 0.583 |
LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.639 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.744 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.826 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.687 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.642 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.689 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.599 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.646 |
MOD_Cter_Amidation | 96 | 99 | PF01082 | 0.659 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.545 |
MOD_GlcNHglycan | 127 | 131 | PF01048 | 0.780 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.688 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.458 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.758 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.658 |
MOD_GlcNHglycan | 302 | 307 | PF01048 | 0.811 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.601 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.549 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.680 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.600 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.776 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.680 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.490 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.460 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.660 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.687 |
MOD_N-GLC_2 | 309 | 311 | PF02516 | 0.645 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.565 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.774 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.661 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.605 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.429 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.708 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.643 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.698 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.728 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.532 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.671 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.597 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.590 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.496 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.728 |
MOD_SUMO_rev_2 | 32 | 40 | PF00179 | 0.595 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICA2 | Leishmania donovani | 100% | 100% |
A4HCG5 | Leishmania braziliensis | 68% | 100% |
E9AVW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4QBL9 | Leishmania major | 87% | 100% |