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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005929 | cilium | 4 | 2 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
GO:0031514 | motile cilium | 5 | 1 |
Related structures:
AlphaFold database: E9AZA0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.773 |
CLV_PCSK_FUR_1 | 129 | 133 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.809 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.789 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.572 |
DEG_SCF_FBW7_1 | 24 | 30 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.569 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.550 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.840 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.720 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.730 |
DOC_USP7_UBL2_3 | 319 | 323 | PF12436 | 0.854 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.840 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.802 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.842 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 204 | 210 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 342 | 349 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.860 |
LIG_14-3-3_CanoR_1 | 98 | 107 | PF00244 | 0.735 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.766 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.820 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.728 |
LIG_BRCT_BRCA1_2 | 424 | 430 | PF00533 | 0.727 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.718 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.616 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.815 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.764 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.778 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.778 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.778 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.778 |
LIG_SH3_1 | 57 | 63 | PF00018 | 0.675 |
LIG_SH3_2 | 60 | 65 | PF14604 | 0.827 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.735 |
MOD_CDC14_SPxK_1 | 18 | 21 | PF00782 | 0.768 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.766 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.659 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.715 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.788 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.758 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.709 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.855 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.707 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.642 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.787 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.577 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.551 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.730 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.754 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.625 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.708 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.630 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.678 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.715 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.677 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.808 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.727 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.712 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.688 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.533 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.641 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.676 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.745 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.813 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.815 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.845 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.625 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.639 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.434 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.549 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.678 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.768 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.593 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.678 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.758 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.856 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.716 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.744 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.744 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.562 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.844 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.685 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.672 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.679 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.686 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.544 |
MOD_SUMO_rev_2 | 407 | 415 | PF00179 | 0.754 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.778 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.657 |
TRG_NLS_Bipartite_1 | 342 | 361 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 354 | 361 | PF00514 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.747 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IE97 | Leishmania donovani | 87% | 100% |
A4HFX1 | Leishmania braziliensis | 60% | 100% |
A4I303 | Leishmania infantum | 87% | 100% |
E9ADH6 | Leishmania major | 84% | 100% |