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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q478
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.363 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 154 | 156 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.522 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.568 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.576 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.644 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.644 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 165 | 173 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.599 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.727 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.542 |
LIG_CaM_IQ_9 | 88 | 103 | PF13499 | 0.491 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.431 |
LIG_RPA_C_Fungi | 85 | 97 | PF08784 | 0.360 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.681 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.605 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.769 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.627 |
LIG_SUMO_SIM_par_1 | 127 | 134 | PF11976 | 0.566 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.593 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.642 |
LIG_UBA3_1 | 115 | 121 | PF00899 | 0.547 |
LIG_UBA3_1 | 321 | 326 | PF00899 | 0.531 |
LIG_WW_3 | 214 | 218 | PF00397 | 0.536 |
MOD_CDK_SPxxK_3 | 192 | 199 | PF00069 | 0.556 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.560 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.701 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.691 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.499 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.407 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.617 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.475 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.632 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.615 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.666 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.587 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.538 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.690 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.721 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.773 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.700 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.685 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.568 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.554 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.641 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.656 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.765 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.614 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.675 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.468 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.619 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.428 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.407 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.682 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.632 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.549 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.600 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.661 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.771 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.734 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.781 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.675 |
MOD_SUMO_rev_2 | 302 | 311 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_1 | 111 | 116 | PF01217 | 0.569 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 104 | 109 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.366 |
TRG_NES_CRM1_1 | 127 | 142 | PF08389 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.464 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE12 | Leptomonas seymouri | 56% | 100% |
A0A1X0P0W7 | Trypanosomatidae | 38% | 100% |
A0A3S7X6M7 | Leishmania donovani | 91% | 100% |
A4HLG6 | Leishmania braziliensis | 63% | 100% |
A4I8X7 | Leishmania infantum | 92% | 100% |
D0A4X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B3U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |