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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AQ49
Term | Name | Level | Count |
---|---|---|---|
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009607 | response to biotic stimulus | 2 | 1 |
GO:0042783 | evasion of host immune response | 6 | 1 |
GO:0042784 | evasion of host immune response via modulation of host complement system | 7 | 1 |
GO:0043207 | response to external biotic stimulus | 3 | 1 |
GO:0044403 | biological process involved in symbiotic interaction | 2 | 1 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051701 | biological process involved in interaction with host | 3 | 1 |
GO:0051707 | response to other organism | 2 | 1 |
GO:0052173 | response to defenses of other organism | 3 | 1 |
GO:0052200 | response to host defenses | 4 | 1 |
GO:0052572 | response to host immune response | 5 | 1 |
GO:0075136 | response to host | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0004857 | enzyme inhibitor activity | 3 | 7 |
GO:0004866 | endopeptidase inhibitor activity | 5 | 7 |
GO:0004867 | serine-type endopeptidase inhibitor activity | 6 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 7 |
GO:0030414 | peptidase inhibitor activity | 4 | 7 |
GO:0061134 | peptidase regulator activity | 3 | 7 |
GO:0061135 | endopeptidase regulator activity | 4 | 7 |
GO:0098772 | molecular function regulator activity | 1 | 7 |
GO:0140678 | molecular function inhibitor activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.494 |
DOC_MAPK_gen_1 | 177 | 183 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.388 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.344 |
DOC_USP7_MATH_2 | 245 | 251 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 127 | 135 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 276 | 283 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 301 | 309 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 321 | 328 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 348 | 357 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.340 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.544 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.388 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.379 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.412 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.431 |
LIG_LIR_Apic_2 | 173 | 179 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.385 |
LIG_MYND_1 | 194 | 198 | PF01753 | 0.639 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.352 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.490 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.304 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.630 |
LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.502 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.300 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.599 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.585 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.633 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.710 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.630 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.469 |
LIG_SUMO_SIM_par_1 | 74 | 80 | PF11976 | 0.315 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.639 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.661 |
MOD_CDC14_SPxK_1 | 353 | 356 | PF00782 | 0.696 |
MOD_CDK_SPK_2 | 284 | 289 | PF00069 | 0.526 |
MOD_CDK_SPK_2 | 350 | 355 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 350 | 356 | PF00069 | 0.677 |
MOD_CDK_SPxxK_3 | 284 | 291 | PF00069 | 0.593 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.702 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.620 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.519 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.608 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.835 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.654 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.632 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.658 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.694 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.657 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.312 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.291 |
MOD_DYRK1A_RPxSP_1 | 350 | 354 | PF00069 | 0.716 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.650 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.536 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.650 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.721 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.808 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.556 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.720 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.727 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.504 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.534 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.663 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.683 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.669 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.665 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.668 |
MOD_LATS_1 | 274 | 280 | PF00433 | 0.562 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.616 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.710 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.606 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.653 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.585 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.388 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.492 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.548 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.568 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.530 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.494 |
MOD_PKA_1 | 253 | 259 | PF00069 | 0.828 |
MOD_PKA_1 | 301 | 307 | PF00069 | 0.711 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.661 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.560 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.635 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.657 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.730 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.700 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.675 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.569 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.340 |
MOD_PKB_1 | 125 | 133 | PF00069 | 0.340 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.511 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.548 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.312 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.260 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.325 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.340 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.315 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.779 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.608 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.743 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.808 |
TRG_NLS_Bipartite_1 | 301 | 322 | PF00514 | 0.713 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ51 | Leptomonas seymouri | 32% | 100% |
A0A3S7WTD9 | Leishmania donovani | 80% | 98% |
A4H824 | Leishmania braziliensis | 45% | 84% |
A4HWF0 | Leishmania infantum | 80% | 98% |
Q4QFD3 | Leishmania major | 82% | 100% |