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: E9AI89
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.716 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.534 |
DEG_SPOP_SBC_1 | 189 | 193 | PF00917 | 0.517 |
DOC_CYCLIN_RxL_1 | 27 | 38 | PF00134 | 0.517 |
DOC_MAPK_gen_1 | 27 | 35 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 220 | 228 | PF00069 | 0.477 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.554 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.572 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 67 | 76 | PF00244 | 0.555 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.520 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.504 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.527 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.710 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.582 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.467 |
LIG_LIR_Gen_1 | 111 | 120 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 146 | 153 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.418 |
LIG_LYPXL_yS_3 | 202 | 205 | PF13949 | 0.391 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.688 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.594 |
LIG_SH3_1 | 132 | 138 | PF00018 | 0.715 |
LIG_SH3_1 | 75 | 81 | PF00018 | 0.701 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.585 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.645 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.530 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.518 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.485 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.712 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.457 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.477 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.407 |
LIG_UBA3_1 | 205 | 210 | PF00899 | 0.335 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.598 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.706 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.448 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.562 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.814 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.547 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.609 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.469 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.526 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.596 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.695 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.510 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.525 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.763 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.617 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.660 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.581 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.533 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.712 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.479 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.556 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.494 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.639 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.615 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.712 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.725 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.585 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.589 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.503 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.514 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.608 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.525 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.489 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.498 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.444 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.470 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.470 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.626 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.480 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.534 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.563 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.535 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.527 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P529 | Leptomonas seymouri | 39% | 100% |
A0A3S7WVT8 | Leishmania donovani | 67% | 100% |
A4HYR9 | Leishmania infantum | 67% | 100% |
E9AUH4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4QD10 | Leishmania major | 66% | 98% |