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: A0A3S7WV91
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_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.297 |
CLV_PCSK_FUR_1 | 125 | 129 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.314 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.346 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.462 |
DOC_MAPK_gen_1 | 148 | 158 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.321 |
DOC_PP1_RVXF_1 | 364 | 370 | PF00149 | 0.423 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.752 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 366 | 370 | PF00244 | 0.423 |
LIG_Actin_WH2_2 | 158 | 173 | PF00022 | 0.426 |
LIG_BIR_III_4 | 284 | 288 | PF00653 | 0.739 |
LIG_eIF4E_1 | 36 | 42 | PF01652 | 0.579 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.400 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.522 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.763 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.756 |
LIG_GBD_Chelix_1 | 158 | 166 | PF00786 | 0.672 |
LIG_IBAR_NPY_1 | 60 | 62 | PF08397 | 0.486 |
LIG_LIR_Apic_2 | 356 | 360 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 407 | 416 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.770 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.631 |
LIG_PDZ_Class_1 | 414 | 419 | PF00595 | 0.648 |
LIG_Pex14_1 | 323 | 327 | PF04695 | 0.747 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.366 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.771 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.512 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.748 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 355 | 358 | PF00017 | 0.562 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.505 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.736 |
MOD_CDK_SPxxK_3 | 118 | 125 | PF00069 | 0.654 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.718 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.728 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.480 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.432 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.456 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.757 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.623 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.602 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.606 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.475 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.637 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.643 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.690 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.519 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.440 |
MOD_CMANNOS | 244 | 247 | PF00535 | 0.496 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.679 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.466 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.636 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.583 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.694 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.659 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.658 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.591 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.660 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.677 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.673 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.675 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.605 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.631 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.533 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.687 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.778 |
MOD_NEK2_2 | 14 | 19 | PF00069 | 0.499 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.710 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.724 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.731 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.758 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.781 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.635 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.698 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.752 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.749 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.252 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.663 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.687 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.675 |
MOD_Plk_2-3 | 315 | 321 | PF00069 | 0.643 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.523 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.472 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.525 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.725 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.670 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.712 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.740 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.577 |
TRG_NES_CRM1_1 | 157 | 168 | PF08389 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 137 | 142 | PF00026 | 0.659 |
TRG_PTS1 | 416 | 419 | PF00515 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9X6 | Leptomonas seymouri | 69% | 99% |
A0A0S4J170 | Bodo saltans | 25% | 92% |
A0A1X0P6F7 | Trypanosomatidae | 35% | 100% |
A0A422NCY3 | Trypanosoma rangeli | 33% | 100% |
A4H9W4 | Leishmania braziliensis | 78% | 100% |
D0A0C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AGQ9 | Leishmania infantum | 100% | 100% |
E9ARV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QDL4 | Leishmania major | 88% | 100% |