Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0030117 | membrane coat | 3 | 3 |
GO:0030118 | clathrin coat | 4 | 3 |
GO:0030120 | vesicle coat | 4 | 3 |
GO:0030125 | clathrin vesicle coat | 5 | 3 |
GO:0030130 | clathrin coat of trans-Golgi network vesicle | 6 | 3 |
GO:0030132 | clathrin coat of coated pit | 4 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0098796 | membrane protein complex | 2 | 3 |
GO:0098797 | plasma membrane protein complex | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S5H749
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006886 | intracellular protein transport | 4 | 3 |
GO:0008104 | protein localization | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015031 | protein transport | 4 | 3 |
GO:0016192 | vesicle-mediated transport | 4 | 3 |
GO:0033036 | macromolecule localization | 2 | 3 |
GO:0045184 | establishment of protein localization | 3 | 3 |
GO:0046907 | intracellular transport | 3 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0051641 | cellular localization | 2 | 3 |
GO:0051649 | establishment of localization in cell | 3 | 3 |
GO:0070727 | cellular macromolecule localization | 3 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.423 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.253 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.253 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.573 |
DOC_CKS1_1 | 272 | 277 | PF01111 | 0.528 |
DOC_CYCLIN_RxL_1 | 52 | 60 | PF00134 | 0.423 |
DOC_MAPK_gen_1 | 55 | 61 | PF00069 | 0.431 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.397 |
DOC_PP4_MxPP_1 | 251 | 254 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.235 |
DOC_USP7_MATH_2 | 275 | 281 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.253 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 382 | 392 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.437 |
LIG_APCC_ABBA_1 | 154 | 159 | PF00400 | 0.580 |
LIG_APCC_ABBA_1 | 59 | 64 | PF00400 | 0.454 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.397 |
LIG_EVH1_1 | 218 | 222 | PF00568 | 0.556 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.502 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 26 | 37 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.387 |
LIG_MLH1_MIPbox_1 | 44 | 48 | PF16413 | 0.397 |
LIG_MYND_1 | 120 | 124 | PF01753 | 0.534 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.400 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.404 |
LIG_SH3_2 | 273 | 278 | PF14604 | 0.513 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.550 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.556 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.574 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.540 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.533 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.534 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.545 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.510 |
LIG_Sin3_3 | 72 | 79 | PF02671 | 0.446 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.584 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.253 |
LIG_TRFH_1 | 37 | 41 | PF08558 | 0.395 |
LIG_UBA3_1 | 364 | 370 | PF00899 | 0.253 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.405 |
LIG_WW_3 | 17 | 21 | PF00397 | 0.427 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.527 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.535 |
MOD_CDK_SPxxK_3 | 271 | 278 | PF00069 | 0.531 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.550 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.525 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.542 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.540 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.253 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.582 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.576 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.567 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.530 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.235 |
MOD_DYRK1A_RPxSP_1 | 271 | 275 | PF00069 | 0.523 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.545 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.526 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.585 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.555 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.568 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.504 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.253 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.239 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.568 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.579 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.575 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.570 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.681 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.246 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.470 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.486 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.568 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.573 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.727 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.395 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.392 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.429 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.416 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.543 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.519 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.567 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.506 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.407 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.552 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.533 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.521 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.572 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.569 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.583 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.559 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.507 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.510 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.401 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.235 |
MOD_SUMO_rev_2 | 307 | 313 | PF00179 | 0.253 |
MOD_SUMO_rev_2 | 347 | 355 | PF00179 | 0.253 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
E9AGR3 | Leishmania infantum | 100% | 100% |