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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q8N9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.511 |
CLV_PCSK_FUR_1 | 301 | 305 | PF00082 | 0.323 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.423 |
DOC_CKS1_1 | 122 | 127 | PF01111 | 0.450 |
DOC_CYCLIN_yCln2_LP_2 | 290 | 296 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 145 | 152 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 227 | 235 | PF00069 | 0.355 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.447 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.355 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.450 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.718 |
LIG_deltaCOP1_diTrp_1 | 243 | 252 | PF00928 | 0.614 |
LIG_deltaCOP1_diTrp_1 | 84 | 92 | PF00928 | 0.670 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.405 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.650 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.757 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.615 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.744 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 269 | 280 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.515 |
LIG_LYPXL_S_1 | 92 | 96 | PF13949 | 0.480 |
LIG_LYPXL_yS_3 | 93 | 96 | PF13949 | 0.480 |
LIG_Pex14_1 | 246 | 250 | PF04695 | 0.602 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.476 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.568 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.628 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.450 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.344 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.426 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.300 |
LIG_SUMO_SIM_anti_2 | 11 | 22 | PF11976 | 0.679 |
LIG_SUMO_SIM_par_1 | 160 | 165 | PF11976 | 0.431 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.440 |
LIG_TYR_ITIM | 99 | 104 | PF00017 | 0.456 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.355 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.362 |
MOD_Cter_Amidation | 131 | 134 | PF01082 | 0.612 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.404 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.503 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.719 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.361 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.661 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.404 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.476 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.419 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.717 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.495 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.713 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.670 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.649 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.755 |
MOD_PKB_1 | 57 | 65 | PF00069 | 0.598 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.748 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.731 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.386 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.706 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.463 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.353 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.358 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.484 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.395 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.361 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.456 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.390 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.488 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.735 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P732 | Leptomonas seymouri | 58% | 92% |
A0A1X0NVF3 | Trypanosomatidae | 34% | 100% |
A0A3Q8IAV0 | Leishmania donovani | 94% | 100% |
A0A3R7KTP8 | Trypanosoma rangeli | 35% | 100% |
A4HG72 | Leishmania braziliensis | 82% | 92% |
A4I3B5 | Leishmania infantum | 94% | 100% |
D0A7T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AZJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DAH6 | Trypanosoma cruzi | 37% | 100% |