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: 5 |
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: A4I6G9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.458 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.391 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.363 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.561 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.502 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.493 |
DOC_PP4_MxPP_1 | 224 | 227 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.582 |
DOC_USP7_UBL2_3 | 130 | 134 | PF12436 | 0.567 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.416 |
LIG_Actin_WH2_2 | 93 | 110 | PF00022 | 0.466 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.444 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.517 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.494 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.366 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.563 |
LIG_Integrin_RGD_1 | 194 | 196 | PF01839 | 0.417 |
LIG_LIR_Apic_2 | 2 | 8 | PF02991 | 0.396 |
LIG_LIR_Apic_2 | 228 | 234 | PF02991 | 0.776 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.430 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.469 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.617 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.612 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.493 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.650 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.542 |
LIG_TRFH_1 | 231 | 235 | PF08558 | 0.601 |
LIG_UBA3_1 | 168 | 177 | PF00899 | 0.450 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.521 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.481 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.676 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.441 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.458 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.544 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.620 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.454 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.454 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.532 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.794 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.581 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.432 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.570 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.428 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.619 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.413 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.391 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.469 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.618 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.429 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.479 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.650 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.514 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.525 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.531 |
MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.524 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.535 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.479 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.472 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.707 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.368 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.384 |
MOD_SUMO_rev_2 | 140 | 148 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 286 | 295 | PF00179 | 0.595 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAJ7 | Leptomonas seymouri | 41% | 100% |
A0A0N1PCN3 | Leptomonas seymouri | 35% | 82% |
A0A3Q8IJW3 | Leishmania donovani | 98% | 100% |
A4HJ55 | Leishmania braziliensis | 65% | 100% |
E9B1M6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q9BHD3 | Leishmania major | 89% | 100% |