Protease inhibitors, Ecotin-like 3 LinJ15.0540 PE=3 SV=1 - [ECOT3_LEIIN]
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) | yes | 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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HWF0
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 | 6 |
GO:0004866 | endopeptidase inhibitor activity | 5 | 6 |
GO:0004867 | serine-type endopeptidase inhibitor activity | 6 | 6 |
GO:0030234 | enzyme regulator activity | 2 | 6 |
GO:0030414 | peptidase inhibitor activity | 4 | 6 |
GO:0061134 | peptidase regulator activity | 3 | 6 |
GO:0061135 | endopeptidase regulator activity | 4 | 6 |
GO:0098772 | molecular function regulator activity | 1 | 6 |
GO:0140678 | molecular function inhibitor activity | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.796 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.647 |
CLV_Separin_Metazoa | 165 | 169 | PF03568 | 0.670 |
DOC_ANK_TNKS_1 | 167 | 174 | PF00023 | 0.587 |
DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.546 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.431 |
DOC_USP7_MATH_2 | 249 | 255 | PF00917 | 0.748 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 269 | 278 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 280 | 290 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 307 | 315 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.338 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.545 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.620 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.603 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.495 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.453 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.492 |
LIG_MYND_1 | 151 | 155 | PF01753 | 0.663 |
LIG_MYND_1 | 198 | 202 | PF01753 | 0.703 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.558 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.684 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.699 |
LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.498 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.520 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.664 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.690 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.739 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.707 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.431 |
LIG_SUMO_SIM_par_1 | 182 | 189 | PF11976 | 0.678 |
LIG_TRAF2_1 | 186 | 189 | PF00917 | 0.715 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.722 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.734 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.320 |
MOD_CDC14_SPxK_1 | 277 | 280 | PF00782 | 0.709 |
MOD_CDC14_SPxK_1 | 359 | 362 | PF00782 | 0.764 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.737 |
MOD_CDK_SPxK_1 | 274 | 280 | PF00069 | 0.709 |
MOD_CDK_SPxK_1 | 356 | 362 | PF00069 | 0.745 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.682 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.577 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.793 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.712 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.592 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.737 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.714 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.729 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.747 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.621 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.504 |
MOD_DYRK1A_RPxSP_1 | 356 | 360 | PF00069 | 0.708 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.721 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.669 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.568 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.777 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.802 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.654 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.504 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.800 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.725 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.617 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.617 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.797 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.748 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.675 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.775 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.463 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.747 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.750 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.658 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.597 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.495 |
MOD_NEK2_2 | 344 | 349 | PF00069 | 0.621 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.623 |
MOD_PKA_1 | 257 | 263 | PF00069 | 0.702 |
MOD_PKA_1 | 307 | 313 | PF00069 | 0.801 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.735 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.700 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.584 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.733 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.780 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.754 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.532 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.431 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.338 |
MOD_PKB_1 | 125 | 133 | PF00069 | 0.495 |
MOD_PKB_1 | 280 | 288 | PF00069 | 0.716 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.583 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.712 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.621 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.558 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.491 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.680 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.412 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.470 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.673 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.804 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.733 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.745 |
MOD_SUMO_rev_2 | 174 | 183 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_4 | 188 | 194 | PF01217 | 0.686 |
TRG_DiLeu_BaEn_4 | 251 | 257 | PF01217 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.704 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.811 |
TRG_NLS_Bipartite_1 | 307 | 328 | PF00514 | 0.801 |
TRG_NLS_MonoExtN_4 | 323 | 328 | PF00514 | 0.712 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTD9 | Leishmania donovani | 99% | 100% |
A4H824 | Leishmania braziliensis | 46% | 82% |
A4HWF0 | Leishmania infantum | 100% | 100% |
E9AQ49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4QFD3 | Leishmania major | 90% | 100% |