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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0012505 | endomembrane system | 2 | 1 |
GO:0031201 | SNARE complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
Related structures:
AlphaFold database: A4H9V8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006906 | vesicle fusion | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016050 | vesicle organization | 5 | 1 |
GO:0022406 | membrane docking | 2 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048278 | vesicle docking | 4 | 1 |
GO:0048284 | organelle fusion | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061025 | membrane fusion | 5 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090174 | organelle membrane fusion | 6 | 1 |
GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005484 | SNAP receptor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.777 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 280 | 286 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.402 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.675 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.643 |
DEG_APCC_KENBOX_2 | 112 | 116 | PF00400 | 0.605 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.705 |
DOC_MAPK_gen_1 | 116 | 127 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 246 | 254 | PF00069 | 0.584 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.710 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.609 |
DOC_USP7_UBL2_3 | 287 | 291 | PF12436 | 0.661 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 135 | 143 | PF00244 | 0.653 |
LIG_AP2alpha_2 | 43 | 45 | PF02296 | 0.604 |
LIG_CaM_IQ_9 | 122 | 138 | PF13499 | 0.598 |
LIG_CaM_IQ_9 | 167 | 183 | PF13499 | 0.708 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.598 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.479 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.672 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.571 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.721 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.606 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.568 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.631 |
LIG_Pex14_2 | 315 | 319 | PF04695 | 0.485 |
LIG_SH2_GRB2like | 139 | 142 | PF00017 | 0.647 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.397 |
LIG_SUMO_SIM_anti_2 | 200 | 205 | PF11976 | 0.778 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.731 |
LIG_UBA3_1 | 182 | 188 | PF00899 | 0.733 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.704 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.701 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.613 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.567 |
MOD_Cter_Amidation | 133 | 136 | PF01082 | 0.440 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.445 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.498 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.590 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.395 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.539 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.585 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.574 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.599 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.537 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.575 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.616 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.543 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.248 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.484 |
MOD_SUMO_for_1 | 231 | 234 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.614 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.582 |
TRG_NLS_Bipartite_1 | 101 | 122 | PF00514 | 0.527 |
TRG_NLS_MonoCore_2 | 115 | 120 | PF00514 | 0.641 |
TRG_NLS_MonoExtC_3 | 115 | 120 | PF00514 | 0.610 |
TRG_NLS_MonoExtN_4 | 113 | 120 | PF00514 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9J7 | Leptomonas seymouri | 75% | 100% |
A0A0S4IV64 | Bodo saltans | 45% | 94% |
A0A0S4IVZ4 | Bodo saltans | 37% | 97% |
A0A0S4IZ68 | Bodo saltans | 45% | 98% |
A0A1X0P6H2 | Trypanosomatidae | 59% | 100% |
A0A3R7LL06 | Trypanosoma rangeli | 53% | 100% |
A0A3S7WV65 | Leishmania donovani | 78% | 100% |
A4HY40 | Leishmania infantum | 78% | 100% |
D0A0C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ARV3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QDM0 | Leishmania major | 76% | 100% |
V5BS89 | Trypanosoma cruzi | 54% | 100% |