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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006901 | vesicle coating | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016050 | vesicle organization | 5 | 1 |
GO:0048200 | Golgi transport vesicle coating | 7 | 1 |
GO:0048205 | COPI coating of Golgi vesicle | 8 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 8 |
GO:0008047 | enzyme activator activity | 3 | 8 |
GO:0030234 | enzyme regulator activity | 2 | 8 |
GO:0030695 | GTPase regulator activity | 4 | 8 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 8 |
GO:0098772 | molecular function regulator activity | 1 | 8 |
GO:0140677 | molecular function activator activity | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.680 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.282 |
DEG_SCF_FBW7_1 | 170 | 177 | PF00400 | 0.663 |
DOC_MAPK_gen_1 | 58 | 66 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 58 | 66 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 78 | 87 | PF00069 | 0.144 |
DOC_MAPK_RevD_3 | 190 | 206 | PF00069 | 0.631 |
DOC_PP1_RVXF_1 | 28 | 34 | PF00149 | 0.349 |
DOC_PP2B_LxvP_1 | 7 | 10 | PF13499 | 0.613 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.349 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.541 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.689 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.403 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.737 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.668 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.704 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.668 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.646 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.698 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.659 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.608 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.326 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.513 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.678 |
LIG_LIR_Apic_2 | 107 | 112 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 41 | 50 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.349 |
LIG_MYND_1 | 356 | 360 | PF01753 | 0.555 |
LIG_PDZ_Class_3 | 437 | 442 | PF00595 | 0.520 |
LIG_PTB_Apo_2 | 375 | 382 | PF02174 | 0.662 |
LIG_PTB_Phospho_1 | 375 | 381 | PF10480 | 0.665 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.649 |
LIG_SH3_1 | 283 | 289 | PF00018 | 0.777 |
LIG_SH3_2 | 326 | 331 | PF14604 | 0.670 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.575 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.777 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.734 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.723 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.594 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.521 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.479 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.675 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.648 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.598 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.571 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.602 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.349 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.504 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.745 |
MOD_DYRK1A_RPxSP_1 | 352 | 356 | PF00069 | 0.704 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.604 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.783 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.687 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.639 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.648 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.562 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.685 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.738 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.580 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.403 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.506 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.637 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.624 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.418 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.716 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.682 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.492 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.349 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.679 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.748 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.738 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.699 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.678 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.579 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.572 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.761 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.670 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.394 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.779 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.403 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.655 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.695 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.487 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.628 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.573 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.591 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.592 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.630 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.738 |
MOD_SUMO_rev_2 | 11 | 19 | PF00179 | 0.462 |
TRG_DiLeu_BaEn_1 | 15 | 20 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.349 |
TRG_NLS_Bipartite_1 | 205 | 223 | PF00514 | 0.639 |
TRG_NLS_MonoExtN_4 | 217 | 223 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 24 | 28 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 374 | 379 | PF00026 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 418 | 422 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I148 | Leptomonas seymouri | 61% | 99% |
A0A0S4JHE6 | Bodo saltans | 38% | 100% |
A1L520 | Bos taurus | 28% | 85% |
A4H760 | Leishmania braziliensis | 77% | 100% |
A4HVJ9 | Leishmania infantum | 100% | 100% |
E9AP95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q28CM8 | Xenopus tropicalis | 28% | 84% |
Q3MID3 | Rattus norvegicus | 27% | 85% |
Q4QG83 | Leishmania major | 91% | 98% |
Q5RAT7 | Pongo abelii | 27% | 85% |
Q8N6H7 | Homo sapiens | 27% | 85% |
Q99K28 | Mus musculus | 27% | 85% |