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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B642
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.528 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.534 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 89 | 95 | PF00134 | 0.503 |
DOC_MIT_MIM_1 | 348 | 357 | PF04212 | 0.534 |
DOC_PP4_FxxP_1 | 145 | 148 | PF00568 | 0.571 |
DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.586 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 151 | 159 | PF00244 | 0.693 |
LIG_Actin_WH2_2 | 294 | 310 | PF00022 | 0.595 |
LIG_Actin_WH2_2 | 68 | 84 | PF00022 | 0.439 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.516 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.574 |
LIG_EH1_1 | 241 | 249 | PF00400 | 0.562 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.488 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.553 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.378 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 143 | 148 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 156 | 162 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.550 |
LIG_MAD2 | 4 | 12 | PF02301 | 0.614 |
LIG_NRBOX | 213 | 219 | PF00104 | 0.536 |
LIG_PDZ_Class_3 | 352 | 357 | PF00595 | 0.594 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.632 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.500 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.634 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.620 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.730 |
LIG_WW_1 | 147 | 150 | PF00397 | 0.651 |
MOD_CDK_SPxxK_3 | 75 | 82 | PF00069 | 0.594 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.654 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.472 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.514 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.650 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.543 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.670 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.726 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.515 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.671 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.560 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.426 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.621 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.660 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.637 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.673 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.743 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.486 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.641 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.573 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.529 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.567 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.454 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.510 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.560 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.494 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.655 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.521 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.658 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.392 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.531 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.596 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.585 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.392 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.683 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.640 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.553 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.608 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKF7 | Leptomonas seymouri | 34% | 100% |
A0A3S7X929 | Leishmania donovani | 85% | 100% |
A4HMI5 | Leishmania braziliensis | 71% | 99% |
A4IB65 | Leishmania infantum | 85% | 100% |
E9AEY6 | Leishmania major | 87% | 100% |