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:0005737 | cytoplasm | 2 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AYJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034067 | protein localization to Golgi apparatus | 6 | 1 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0072659 | protein localization to plasma membrane | 5 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 1 |
GO:1990778 | protein localization to cell periphery | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0003924 | GTPase activity | 7 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005525 | GTP binding | 5 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0019001 | guanyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 120 | 126 | PF00089 | 0.431 |
CLV_MEL_PAP_1 | 354 | 360 | PF00089 | 0.594 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.705 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 175 | 183 | PF00400 | 0.360 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.440 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.498 |
DOC_CDC14_PxL_1 | 259 | 267 | PF14671 | 0.366 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.489 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.486 |
DOC_CKS1_1 | 77 | 82 | PF01111 | 0.813 |
DOC_CKS1_1 | 93 | 98 | PF01111 | 0.425 |
DOC_CYCLIN_yCln2_LP_2 | 254 | 260 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 107 | 115 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 135 | 141 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 107 | 115 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 350 | 358 | PF00069 | 0.544 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.568 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 56 | 66 | PF00244 | 0.613 |
LIG_EVH1_1 | 147 | 151 | PF00568 | 0.542 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.412 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.416 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.495 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.726 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.526 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.451 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.336 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.659 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.700 |
LIG_GBD_Chelix_1 | 202 | 210 | PF00786 | 0.376 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 17 | 23 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 361 | 366 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.542 |
LIG_NRBOX | 249 | 255 | PF00104 | 0.443 |
LIG_PCNA_PIPBox_1 | 185 | 194 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 180 | 192 | PF02747 | 0.360 |
LIG_PDZ_Class_1 | 398 | 403 | PF00595 | 0.553 |
LIG_Pex14_1 | 192 | 196 | PF04695 | 0.300 |
LIG_PTB_Apo_2 | 7 | 14 | PF02174 | 0.536 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.454 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.333 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 117 | 121 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.479 |
LIG_SH3_1 | 87 | 93 | PF00018 | 0.638 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.658 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.692 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.774 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.621 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 262 | 268 | PF11976 | 0.356 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.501 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.426 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.686 |
LIG_TYR_ITIM | 115 | 120 | PF00017 | 0.454 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.398 |
LIG_WW_3 | 228 | 232 | PF00397 | 0.567 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.535 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.700 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.635 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.630 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.471 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.788 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.606 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.519 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.699 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.500 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.460 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.338 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.661 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.270 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.653 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.691 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.578 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.412 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.792 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.512 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.717 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.544 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.406 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.622 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.510 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.579 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.293 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.473 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.648 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.766 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.534 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.438 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.601 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.446 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.369 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.525 |
MOD_NEK2_2 | 364 | 369 | PF00069 | 0.502 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.633 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.360 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.660 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.498 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.413 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.354 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.602 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.303 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.496 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.442 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.366 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.591 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.397 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.665 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.524 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.478 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.498 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.465 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.576 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.579 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.634 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.480 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.813 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.440 |
MOD_SUMO_rev_2 | 232 | 242 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 34 | 40 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.487 |
TRG_NLS_MonoExtC_3 | 106 | 111 | PF00514 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 180 | 185 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTD1 | Leptomonas seymouri | 58% | 100% |
A0A3Q8ICC5 | Leishmania donovani | 92% | 100% |
A4HF63 | Leishmania braziliensis | 71% | 98% |
A4I2E6 | Leishmania infantum | 92% | 100% |
C9ZX62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4Q8X3 | Leishmania major | 90% | 100% |