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:0012505 | endomembrane system | 2 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0031201 | SNARE complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QIZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006906 | vesicle fusion | 6 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016050 | vesicle organization | 5 | 2 |
GO:0022406 | membrane docking | 2 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0048278 | vesicle docking | 4 | 2 |
GO:0048284 | organelle fusion | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0061025 | membrane fusion | 5 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090174 | organelle membrane fusion | 6 | 2 |
GO:0140056 | organelle localization by membrane tethering | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 2 |
GO:0005484 | SNAP receptor activity | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.447 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 139 | 145 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.393 |
DEG_APCC_DBOX_1 | 67 | 75 | PF00400 | 0.574 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.732 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.734 |
DOC_CYCLIN_yCln2_LP_2 | 227 | 233 | PF00134 | 0.793 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.663 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.665 |
LIG_14-3-3_CterR_2 | 394 | 397 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 378 | 396 | PF00022 | 0.402 |
LIG_Actin_WH2_2 | 57 | 74 | PF00022 | 0.580 |
LIG_CaM_IQ_9 | 354 | 370 | PF13499 | 0.667 |
LIG_Clathr_ClatBox_1 | 284 | 288 | PF01394 | 0.738 |
LIG_EH1_1 | 377 | 385 | PF00400 | 0.447 |
LIG_eIF4E_1 | 378 | 384 | PF01652 | 0.447 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.695 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.689 |
LIG_GBD_Chelix_1 | 379 | 387 | PF00786 | 0.480 |
LIG_LIR_Gen_1 | 298 | 305 | PF02991 | 0.585 |
LIG_LIR_LC3C_4 | 333 | 337 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.570 |
LIG_MAD2 | 215 | 223 | PF02301 | 0.665 |
LIG_NRBOX | 381 | 387 | PF00104 | 0.447 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.447 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.622 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.378 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.793 |
LIG_SUMO_SIM_par_1 | 282 | 289 | PF11976 | 0.675 |
LIG_Vh1_VBS_1 | 377 | 395 | PF01044 | 0.441 |
MOD_CDK_SPxK_1 | 48 | 54 | PF00069 | 0.596 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.652 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.608 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.783 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.685 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.731 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.664 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.570 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.602 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.669 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.544 |
MOD_Cter_Amidation | 81 | 84 | PF01082 | 0.539 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.703 |
MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.691 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.684 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.620 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.752 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.617 |
MOD_GlcNHglycan | 346 | 350 | PF01048 | 0.447 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.591 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.644 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.665 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.654 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.462 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.607 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.535 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.548 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.501 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.550 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.522 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.358 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.591 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.746 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.481 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.561 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.550 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.638 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.568 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.509 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.698 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.690 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.678 |
TRG_DiLeu_BaLyEn_6 | 280 | 285 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.563 |
TRG_DiLeu_LyEn_5 | 108 | 113 | PF01217 | 0.633 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P557 | Leptomonas seymouri | 46% | 88% |
A0A0S4JA95 | Bodo saltans | 27% | 100% |
A0A1X0NMF9 | Trypanosomatidae | 27% | 100% |
A0A3S7WPJ4 | Leishmania donovani | 87% | 96% |
A0A422NZG0 | Trypanosoma rangeli | 29% | 100% |
A4H4P4 | Leishmania braziliensis | 72% | 97% |
A4HSX4 | Leishmania infantum | 87% | 96% |
E9AKW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
V5BT43 | Trypanosoma cruzi | 30% | 90% |