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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
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: A4H4P4
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_NRD_NRD_1 | 117 | 119 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 200 | 204 | PF00082 | 0.298 |
CLV_PCSK_FUR_1 | 375 | 379 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.308 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.367 |
DEG_APCC_DBOX_1 | 69 | 77 | PF00400 | 0.576 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.705 |
DEG_SCF_FBW7_1 | 178 | 183 | PF00400 | 0.560 |
DEG_SPOP_SBC_1 | 171 | 175 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.561 |
DOC_CYCLIN_yCln2_LP_2 | 224 | 230 | PF00134 | 0.703 |
DOC_MAPK_gen_1 | 2 | 13 | PF00069 | 0.675 |
DOC_MAPK_gen_1 | 202 | 213 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.594 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.583 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 126 | 133 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 160 | 170 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 1 | 16 | PF00022 | 0.583 |
LIG_Actin_WH2_2 | 287 | 303 | PF00022 | 0.552 |
LIG_Actin_WH2_2 | 59 | 76 | PF00022 | 0.547 |
LIG_BIR_III_4 | 81 | 85 | PF00653 | 0.522 |
LIG_CaM_IQ_9 | 367 | 383 | PF13499 | 0.578 |
LIG_EH1_1 | 390 | 398 | PF00400 | 0.410 |
LIG_eIF4E_1 | 391 | 397 | PF01652 | 0.410 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.634 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.626 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.614 |
LIG_GBD_Chelix_1 | 392 | 400 | PF00786 | 0.355 |
LIG_LIR_Gen_1 | 311 | 321 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 59 | 67 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.531 |
LIG_NRBOX | 394 | 400 | PF00104 | 0.430 |
LIG_NRBOX | 401 | 407 | PF00104 | 0.402 |
LIG_Pex14_2 | 309 | 313 | PF04695 | 0.589 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.487 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.789 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.584 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.662 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.597 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.765 |
LIG_Vh1_VBS_1 | 390 | 408 | PF01044 | 0.330 |
MOD_CDK_SPxK_1 | 50 | 56 | PF00069 | 0.647 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.628 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.741 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.718 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.742 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.755 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.708 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.663 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.588 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.758 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.390 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.568 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.511 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.419 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.540 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.573 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.523 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.517 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.666 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.722 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.565 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.708 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.610 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.610 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.608 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.669 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.589 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.573 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.594 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.579 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.547 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.585 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.543 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.577 |
MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.702 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.626 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.662 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.660 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.609 |
MOD_SUMO_rev_2 | 90 | 100 | PF00179 | 0.603 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.700 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.526 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 6 | 10 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P557 | Leptomonas seymouri | 44% | 91% |
A0A0S4JA95 | Bodo saltans | 24% | 100% |
A0A1X0NMF9 | Trypanosomatidae | 27% | 100% |
A0A3S7WPJ4 | Leishmania donovani | 76% | 100% |
A0A422NZG0 | Trypanosoma rangeli | 31% | 100% |
A4HSX4 | Leishmania infantum | 76% | 100% |
E9AKW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QIZ5 | Leishmania major | 72% | 100% |
V5BT43 | Trypanosoma cruzi | 31% | 93% |