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: E9ARV8
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 | 86 | 90 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.314 |
CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.631 |
CLV_PCSK_FUR_1 | 282 | 286 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.547 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.346 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.448 |
DOC_MAPK_gen_1 | 156 | 166 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 251 | 259 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 253 | 261 | PF00069 | 0.321 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 334 | 341 | PF00244 | 0.611 |
LIG_Actin_WH2_2 | 166 | 181 | PF00022 | 0.419 |
LIG_BIR_III_4 | 292 | 296 | PF00653 | 0.736 |
LIG_EH_1 | 67 | 71 | PF12763 | 0.371 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.578 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.426 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.572 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.380 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.754 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.749 |
LIG_GBD_Chelix_1 | 166 | 174 | PF00786 | 0.662 |
LIG_LIR_Gen_1 | 236 | 244 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.763 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.562 |
LIG_PDZ_Class_1 | 422 | 427 | PF00595 | 0.646 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.748 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.363 |
LIG_PTB_Apo_2 | 64 | 71 | PF02174 | 0.452 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.762 |
LIG_SH2_SRC | 388 | 391 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.736 |
LIG_SH2_STAP1 | 363 | 367 | PF00017 | 0.548 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.562 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.484 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.731 |
MOD_CDK_SPxxK_3 | 126 | 133 | PF00069 | 0.638 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.711 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.715 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.432 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.396 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.729 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.587 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.433 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.632 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.683 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.507 |
MOD_CMANNOS | 252 | 255 | PF00535 | 0.497 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.428 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.451 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.592 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.630 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.561 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.715 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.656 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.648 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.649 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.672 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.734 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.658 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.595 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.653 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.550 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.686 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.764 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.696 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.714 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.720 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.770 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.781 |
MOD_PKA_1 | 284 | 290 | PF00069 | 0.594 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.623 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.691 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.739 |
MOD_PKB_1 | 282 | 290 | PF00069 | 0.606 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.650 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.674 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.655 |
MOD_Plk_2-3 | 323 | 329 | PF00069 | 0.630 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.538 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.428 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.628 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.733 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.655 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.729 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 165 | 176 | PF08389 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 145 | 150 | PF00026 | 0.633 |
TRG_PTS1 | 424 | 427 | PF00515 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9X6 | Leptomonas seymouri | 71% | 100% |
A0A0S4J170 | Bodo saltans | 24% | 94% |
A0A1X0P6F7 | Trypanosomatidae | 34% | 100% |
A0A3S7WV91 | Leishmania donovani | 87% | 100% |
A0A422NCY3 | Trypanosoma rangeli | 32% | 100% |
A4H9W4 | Leishmania braziliensis | 79% | 100% |
D0A0C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AGQ9 | Leishmania infantum | 90% | 100% |
Q4QDL4 | Leishmania major | 90% | 100% |