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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I9C9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.739 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.696 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.684 |
CLV_PCSK_FUR_1 | 384 | 388 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.675 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 382 | 388 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.460 |
CLV_Separin_Metazoa | 179 | 183 | PF03568 | 0.591 |
CLV_Separin_Metazoa | 262 | 266 | PF03568 | 0.646 |
DOC_ANK_TNKS_1 | 388 | 395 | PF00023 | 0.654 |
DOC_PP1_RVXF_1 | 332 | 339 | PF00149 | 0.553 |
DOC_PP4_FxxP_1 | 385 | 388 | PF00568 | 0.696 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.674 |
DOC_USP7_UBL2_3 | 186 | 190 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.760 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.681 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.782 |
LIG_BIR_III_4 | 146 | 150 | PF00653 | 0.657 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.668 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.738 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.602 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.651 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.617 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.681 |
LIG_LYPXL_yS_3 | 59 | 62 | PF13949 | 0.637 |
LIG_PCNA_PIPBox_1 | 326 | 335 | PF02747 | 0.571 |
LIG_PCNA_yPIPBox_3 | 167 | 181 | PF02747 | 0.598 |
LIG_PCNA_yPIPBox_3 | 326 | 337 | PF02747 | 0.583 |
LIG_RPA_C_Fungi | 132 | 144 | PF08784 | 0.666 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 104 | 108 | PF00017 | 0.706 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.681 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.506 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.712 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.580 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.593 |
LIG_Sin3_3 | 140 | 147 | PF02671 | 0.668 |
LIG_SUMO_SIM_par_1 | 297 | 306 | PF11976 | 0.599 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.613 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.764 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.708 |
LIG_ULM_U2AF65_1 | 334 | 339 | PF00076 | 0.556 |
LIG_WW_3 | 14 | 18 | PF00397 | 0.770 |
MOD_CDC14_SPxK_1 | 14 | 17 | PF00782 | 0.773 |
MOD_CDK_SPxK_1 | 11 | 17 | PF00069 | 0.777 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.719 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.718 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.622 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.738 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.601 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.566 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.648 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.568 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.735 |
MOD_Cter_Amidation | 226 | 229 | PF01082 | 0.507 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.643 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.701 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.770 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.630 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.643 |
MOD_GlcNHglycan | 273 | 277 | PF01048 | 0.482 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.700 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.728 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.733 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.649 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.541 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.694 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.771 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.667 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.758 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.636 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.660 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.521 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.758 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.699 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.616 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.766 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.557 |
MOD_PKA_1 | 194 | 200 | PF00069 | 0.676 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.723 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.643 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.735 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.655 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.777 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.720 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.760 |
MOD_SUMO_for_1 | 371 | 374 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 254 | 263 | PF00179 | 0.623 |
TRG_DiLeu_BaEn_4 | 259 | 265 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.706 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.652 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.682 |
TRG_NLS_Bipartite_1 | 317 | 338 | PF00514 | 0.666 |
TRG_NLS_MonoExtC_3 | 185 | 190 | PF00514 | 0.454 |
TRG_NLS_MonoExtC_3 | 227 | 233 | PF00514 | 0.639 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L6 | Leptomonas seymouri | 57% | 100% |
A0A3S7X784 | Leishmania donovani | 100% | 100% |
A4HLZ9 | Leishmania braziliensis | 79% | 100% |
E9B4C9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q3P7 | Leishmania major | 89% | 100% |
V5BJN0 | Trypanosoma cruzi | 27% | 100% |