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: A0A3Q8ICC5
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_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.415 |
CLV_MEL_PAP_1 | 121 | 127 | PF00089 | 0.436 |
CLV_MEL_PAP_1 | 355 | 361 | PF00089 | 0.566 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.685 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.588 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.360 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.430 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.497 |
DOC_CDC14_PxL_1 | 260 | 268 | PF14671 | 0.363 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.494 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.496 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.725 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 255 | 261 | PF00134 | 0.460 |
DOC_MAPK_gen_1 | 108 | 116 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 136 | 142 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 351 | 359 | PF00069 | 0.531 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.569 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.439 |
LIG_14-3-3_CanoR_1 | 214 | 223 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.592 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.421 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.409 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.474 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.425 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.712 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.520 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.441 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.363 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.652 |
LIG_GBD_Chelix_1 | 203 | 211 | PF00786 | 0.376 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 17 | 23 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 362 | 367 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.542 |
LIG_NRBOX | 250 | 256 | PF00104 | 0.430 |
LIG_PCNA_PIPBox_1 | 186 | 195 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 181 | 193 | PF02747 | 0.360 |
LIG_PDZ_Class_1 | 399 | 404 | PF00595 | 0.547 |
LIG_Pex14_1 | 193 | 197 | PF04695 | 0.300 |
LIG_PTB_Apo_2 | 7 | 14 | PF02174 | 0.532 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.458 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.344 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 118 | 122 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.525 |
LIG_SH2_STAT3 | 299 | 302 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.489 |
LIG_SH3_1 | 88 | 94 | PF00018 | 0.642 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.613 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.629 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.738 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 130 | 136 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 370 | 375 | PF11976 | 0.413 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.494 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.415 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.642 |
LIG_TYR_ITIM | 116 | 121 | PF00017 | 0.452 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.382 |
LIG_WW_3 | 229 | 233 | PF00397 | 0.568 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.642 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.676 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.479 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.614 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.448 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.714 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.570 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.512 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.708 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.493 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.452 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.251 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.654 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.592 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.620 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.395 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.802 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.630 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.472 |
MOD_GlcNHglycan | 373 | 377 | PF01048 | 0.360 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.722 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.475 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.552 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.281 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.469 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.639 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.720 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.534 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.435 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.599 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.446 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.366 |
MOD_NEK2_2 | 365 | 370 | PF00069 | 0.459 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.484 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.622 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.360 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.710 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.535 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.430 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.354 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.586 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.300 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.492 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.438 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.357 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.590 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.406 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.635 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.525 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.474 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.517 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.441 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.572 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.766 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.490 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.724 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.430 |
MOD_SUMO_rev_2 | 233 | 243 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_2 | 34 | 40 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.675 |
TRG_NLS_MonoExtC_3 | 107 | 112 | PF00514 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTD1 | Leptomonas seymouri | 58% | 100% |
A4HF63 | Leishmania braziliensis | 71% | 98% |
A4I2E6 | Leishmania infantum | 100% | 100% |
C9ZX62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AYJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q8X3 | Leishmania major | 94% | 100% |