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: Q4QFD3
Term | Name | Level | Count |
---|---|---|---|
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009607 | response to biotic stimulus | 2 | 2 |
GO:0042783 | evasion of host immune response | 6 | 2 |
GO:0042784 | evasion of host immune response via modulation of host complement system | 7 | 2 |
GO:0043207 | response to external biotic stimulus | 3 | 2 |
GO:0044403 | biological process involved in symbiotic interaction | 2 | 2 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051701 | biological process involved in interaction with host | 3 | 2 |
GO:0051707 | response to other organism | 2 | 2 |
GO:0052173 | response to defenses of other organism | 3 | 2 |
GO:0052200 | response to host defenses | 4 | 2 |
GO:0052572 | response to host immune response | 5 | 2 |
GO:0075136 | response to host | 3 | 2 |
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 | 0.323 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.709 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.515 |
CLV_Separin_Metazoa | 165 | 169 | PF03568 | 0.642 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.576 |
DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.466 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.330 |
DOC_USP7_MATH_2 | 249 | 255 | PF00917 | 0.717 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 127 | 135 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 268 | 277 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 306 | 314 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.295 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.558 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.511 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.414 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.376 |
LIG_MYND_1 | 151 | 155 | PF01753 | 0.642 |
LIG_MYND_1 | 198 | 202 | PF01753 | 0.652 |
LIG_Pex14_1 | 69 | 73 | PF04695 | 0.339 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.348 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 287 | 290 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.508 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.326 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.640 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.647 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.717 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.670 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.484 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.640 |
LIG_SUMO_SIM_par_1 | 74 | 80 | PF11976 | 0.366 |
LIG_TRAF2_1 | 186 | 189 | PF00917 | 0.674 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.687 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.705 |
MOD_CDC14_SPxK_1 | 276 | 279 | PF00782 | 0.672 |
MOD_CDC14_SPxK_1 | 358 | 361 | PF00782 | 0.738 |
MOD_CDK_SPK_2 | 318 | 323 | PF00069 | 0.572 |
MOD_CDK_SPK_2 | 355 | 360 | PF00069 | 0.733 |
MOD_CDK_SPxK_1 | 273 | 279 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.612 |
MOD_CDK_SPxK_1 | 355 | 361 | PF00069 | 0.719 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.644 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.536 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.799 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.695 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.622 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.804 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.656 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.678 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.662 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.703 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.339 |
MOD_DYRK1A_RPxSP_1 | 355 | 359 | PF00069 | 0.682 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.668 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.598 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.540 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.747 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.649 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.650 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.515 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.817 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.725 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.586 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.647 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.568 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.687 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.554 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.634 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.658 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.433 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.545 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.613 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.591 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.739 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.721 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.627 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.552 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.466 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.586 |
MOD_PKA_1 | 306 | 312 | PF00069 | 0.777 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.701 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.673 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.617 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.760 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.729 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.639 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.399 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.324 |
MOD_PKB_1 | 125 | 133 | PF00069 | 0.399 |
MOD_PKB_1 | 279 | 287 | PF00069 | 0.678 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.561 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.682 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.607 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.339 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.646 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.379 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.484 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.313 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.637 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.793 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.741 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.612 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 173 | 183 | PF00179 | 0.641 |
TRG_DiLeu_BaEn_4 | 188 | 194 | PF01217 | 0.652 |
TRG_DiLeu_BaEn_4 | 251 | 257 | PF01217 | 0.682 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.790 |
TRG_NLS_Bipartite_1 | 306 | 327 | PF00514 | 0.773 |
TRG_NLS_MonoExtN_4 | 322 | 327 | PF00514 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ51 | Leptomonas seymouri | 34% | 100% |
A0A3S7WTD9 | Leishmania donovani | 90% | 100% |
A4H824 | Leishmania braziliensis | 46% | 100% |
A4HWF0 | Leishmania infantum | 90% | 100% |
E9AQ49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QFD3 | Leishmania major | 100% | 100% |