Membrane associated proteins, YIPF
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3Q8IBR6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0019899 | enzyme binding | 3 | 12 |
GO:0031267 | small GTPase binding | 5 | 12 |
GO:0051020 | GTPase binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.278 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.286 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.497 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 249 | 258 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.417 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.453 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 132 | 138 | PF00244 | 0.510 |
LIG_Actin_WH2_2 | 117 | 134 | PF00022 | 0.482 |
LIG_AP2alpha_2 | 12 | 14 | PF02296 | 0.597 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.607 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.607 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.274 |
LIG_deltaCOP1_diTrp_1 | 315 | 325 | PF00928 | 0.457 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.489 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.664 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.299 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.453 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.278 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.753 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.598 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.449 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.510 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.684 |
LIG_IBAR_NPY_1 | 3 | 5 | PF08397 | 0.601 |
LIG_LIR_Apic_2 | 110 | 116 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 192 | 201 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.198 |
LIG_LIR_Gen_1 | 49 | 59 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.188 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.723 |
LIG_PALB2_WD40_1 | 314 | 322 | PF16756 | 0.510 |
LIG_PDZ_Class_2 | 341 | 346 | PF00595 | 0.280 |
LIG_Pex14_1 | 113 | 117 | PF04695 | 0.478 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.206 |
LIG_Pex14_1 | 297 | 301 | PF04695 | 0.256 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.465 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.312 |
LIG_Pex14_2 | 325 | 329 | PF04695 | 0.360 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.250 |
LIG_REV1ctd_RIR_1 | 339 | 346 | PF16727 | 0.372 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.406 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.350 |
LIG_SH2_NCK_1 | 231 | 235 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 52 | 56 | PF00017 | 0.643 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.217 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.235 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.654 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.519 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.648 |
LIG_SUMO_SIM_anti_2 | 197 | 202 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 196 | 202 | PF11976 | 0.335 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.648 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.386 |
LIG_TYR_ITSM | 297 | 304 | PF00017 | 0.335 |
LIG_UBA3_1 | 204 | 212 | PF00899 | 0.306 |
LIG_UBA3_1 | 302 | 311 | PF00899 | 0.306 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.711 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.223 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.699 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.680 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.627 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.510 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.685 |
MOD_CMANNOS | 307 | 310 | PF00535 | 0.217 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.507 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.490 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.451 |
MOD_GlcNHglycan | 75 | 79 | PF01048 | 0.429 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.615 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.268 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.260 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.453 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.726 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.705 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.638 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.431 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.519 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.465 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.662 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.291 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.447 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.455 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.275 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.249 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.685 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.182 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.477 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.637 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.685 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.210 |
MOD_Plk_2-3 | 167 | 173 | PF00069 | 0.650 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.484 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.254 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.308 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.664 |
TRG_DiLeu_BaEn_2 | 314 | 320 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.770 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG17 | Leptomonas seymouri | 62% | 95% |
A0A0S4JRK9 | Bodo saltans | 62% | 100% |
A0A1X0P3E9 | Trypanosomatidae | 49% | 95% |
A0A422N136 | Trypanosoma rangeli | 49% | 99% |
A4HHV9 | Leishmania braziliensis | 90% | 100% |
A4I509 | Leishmania infantum | 100% | 100% |
C9ZQG2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 97% |
E9B0D9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q7U1 | Leishmania major | 96% | 100% |
Q54TS4 | Dictyostelium discoideum | 30% | 100% |
Q5RBL0 | Pongo abelii | 28% | 100% |
Q6P6G5 | Rattus norvegicus | 27% | 100% |
Q91VU1 | Mus musculus | 27% | 100% |
Q9UTD3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q9Y548 | Homo sapiens | 28% | 100% |
V5BLF2 | Trypanosoma cruzi | 48% | 100% |