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:0005778 | peroxisomal membrane | 6 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 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:0046860 | glycosome membrane | 7 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H9W4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 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:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.248 |
CLV_PCSK_FUR_1 | 102 | 106 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.287 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.351 |
DOC_MAPK_gen_1 | 125 | 135 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 222 | 230 | PF00069 | 0.256 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.506 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 311 | 318 | PF00244 | 0.576 |
LIG_Actin_WH2_2 | 135 | 150 | PF00022 | 0.356 |
LIG_eIF4E_1 | 18 | 24 | PF01652 | 0.440 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.340 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.555 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.204 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.650 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.690 |
LIG_GBD_Chelix_1 | 135 | 143 | PF00786 | 0.679 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.380 |
LIG_PDZ_Class_1 | 391 | 396 | PF00595 | 0.578 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.296 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.625 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.513 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.435 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.445 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.183 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.554 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.516 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.652 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.627 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.582 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.509 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.341 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.547 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.604 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.368 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.505 |
MOD_CMANNOS | 221 | 224 | PF00535 | 0.408 |
MOD_Cter_Amidation | 376 | 379 | PF01082 | 0.348 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.418 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.495 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.569 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.565 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.476 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.435 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.554 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.555 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.640 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.266 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.549 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.631 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.559 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.574 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.681 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.266 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.474 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.262 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.579 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.593 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.713 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.649 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.183 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.467 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.365 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.522 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.530 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.558 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.750 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.662 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.555 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.579 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.361 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.432 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.540 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.497 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.183 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.656 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 134 | 145 | PF08389 | 0.404 |
TRG_NLS_MonoExtN_4 | 218 | 223 | PF00514 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.568 |
TRG_PTS1 | 393 | 396 | PF00515 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9X6 | Leptomonas seymouri | 68% | 93% |
A0A0S4J170 | Bodo saltans | 24% | 87% |
A0A1X0P6F7 | Trypanosomatidae | 34% | 100% |
A0A3S7WV91 | Leishmania donovani | 78% | 95% |
A0A422NCY3 | Trypanosoma rangeli | 31% | 100% |
D0A0C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGQ9 | Leishmania infantum | 79% | 93% |
E9ARV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 93% |
Q4QDL4 | Leishmania major | 78% | 100% |