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:0031080 | nuclear pore outer ring | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0035859 | Seh1-associated complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HK41
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009966 | regulation of signal transduction | 4 | 11 |
GO:0009967 | positive regulation of signal transduction | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010646 | regulation of cell communication | 4 | 11 |
GO:0010647 | positive regulation of cell communication | 5 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0023051 | regulation of signaling | 3 | 11 |
GO:0023056 | positive regulation of signaling | 4 | 11 |
GO:0032006 | regulation of TOR signaling | 6 | 11 |
GO:0032008 | positive regulation of TOR signaling | 7 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0048518 | positive regulation of biological process | 3 | 11 |
GO:0048522 | positive regulation of cellular process | 4 | 11 |
GO:0048583 | regulation of response to stimulus | 3 | 11 |
GO:0048584 | positive regulation of response to stimulus | 4 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 11 |
GO:1902533 | positive regulation of intracellular signal transduction | 6 | 11 |
GO:1903432 | regulation of TORC1 signaling | 7 | 11 |
GO:1904263 | positive regulation of TORC1 signaling | 8 | 11 |
GO:0006950 | response to stress | 2 | 1 |
GO:0007154 | cell communication | 2 | 1 |
GO:0009267 | cellular response to starvation | 4 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009991 | response to extracellular stimulus | 3 | 1 |
GO:0031667 | response to nutrient levels | 4 | 1 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 1 |
GO:0031669 | cellular response to nutrient levels | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034198 | cellular response to amino acid starvation | 5 | 1 |
GO:0042594 | response to starvation | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071496 | cellular response to external stimulus | 3 | 1 |
GO:1990928 | response to amino acid starvation | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.536 |
DOC_MAPK_gen_1 | 284 | 291 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 294 | 302 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.508 |
DOC_MAPK_RevD_3 | 297 | 313 | PF00069 | 0.526 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.257 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.369 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 268 | 272 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 343 | 350 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 38 | 42 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 252 | 270 | PF00022 | 0.568 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.523 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.343 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.447 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.568 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.540 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.504 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.250 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.494 |
LIG_LIR_Apic_2 | 316 | 321 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 251 | 262 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.339 |
LIG_Pex14_1 | 84 | 88 | PF04695 | 0.344 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.508 |
LIG_PTB_Apo_2 | 116 | 123 | PF02174 | 0.253 |
LIG_REV1ctd_RIR_1 | 240 | 250 | PF16727 | 0.410 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.519 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.483 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.414 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.370 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.491 |
LIG_SUMO_SIM_par_1 | 230 | 237 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.441 |
MOD_CDC14_SPxK_1 | 107 | 110 | PF00782 | 0.523 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.511 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.345 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.555 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.687 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.448 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.498 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.364 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.361 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.466 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.462 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.512 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.514 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.475 |
MOD_Cter_Amidation | 282 | 285 | PF01082 | 0.532 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.661 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.261 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.621 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.658 |
MOD_GlcNHglycan | 198 | 203 | PF01048 | 0.685 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.352 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.357 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.170 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.522 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.471 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.395 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.451 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.474 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.660 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.419 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.468 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.301 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.333 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.381 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.527 |
MOD_LATS_1 | 37 | 43 | PF00433 | 0.502 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.467 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.500 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.342 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.596 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.461 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.506 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.460 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.321 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.425 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.556 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.525 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.532 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.495 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.498 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.437 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.432 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.368 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.527 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.536 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.507 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.490 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.401 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.513 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.499 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.515 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.630 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.377 |
MOD_SUMO_rev_2 | 306 | 314 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_1 | 96 | 101 | PF01217 | 0.536 |
TRG_DiLeu_LyEn_5 | 71 | 76 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM52 | Leptomonas seymouri | 74% | 98% |
A0A1X0NW55 | Trypanosomatidae | 47% | 100% |
A0A3Q8IKQ4 | Leishmania donovani | 89% | 100% |
A0A3S5IRB2 | Trypanosoma rangeli | 45% | 100% |
A4I7M1 | Leishmania infantum | 89% | 100% |
C1BK83 | Osmerus mordax | 25% | 100% |
D0A9S7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B2I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q5M2 | Leishmania major | 88% | 98% |
Q6BZX5 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 22% | 100% |
Q6CSZ5 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 22% | 100% |
Q6FNV4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 100% |
Q6TGU2 | Danio rerio | 25% | 100% |
Q75BS2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 22% | 100% |
Q7K2X8 | Drosophila melanogaster | 25% | 100% |
V5BFB9 | Trypanosoma cruzi | 45% | 100% |