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 |
Related structures:
AlphaFold database: A4I6V3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 269 | 271 | PF00082 | 0.717 |
CLV_PCSK_PC7_1 | 124 | 130 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 185 | 191 | PF00082 | 0.609 |
CLV_PCSK_PC7_1 | 84 | 90 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.808 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.706 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.781 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 84 | 94 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 88 | 96 | PF00069 | 0.609 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.669 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.682 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.738 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.784 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 88 | 96 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 73 | 90 | PF00022 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.787 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.787 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.759 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.595 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.744 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.586 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.698 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.709 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.608 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.759 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.694 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.635 |
LIG_Integrin_RGD_1 | 164 | 166 | PF01839 | 0.766 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.688 |
LIG_LIR_Apic_2 | 365 | 371 | PF02991 | 0.640 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 213 | 224 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.607 |
LIG_PCNA_PIPBox_1 | 80 | 89 | PF02747 | 0.652 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.749 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.661 |
LIG_SH3_1 | 192 | 198 | PF00018 | 0.728 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.665 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.673 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.650 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.630 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.670 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.715 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.655 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.643 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.780 |
LIG_SUMO_SIM_anti_2 | 104 | 109 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.692 |
MOD_CDC14_SPxK_1 | 22 | 25 | PF00782 | 0.779 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.783 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.770 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.754 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.726 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.528 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.711 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.707 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.570 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.739 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.576 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.760 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.631 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.661 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.567 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.714 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.678 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.724 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.687 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.694 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.534 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.674 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.706 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.788 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.767 |
MOD_LATS_1 | 359 | 365 | PF00433 | 0.631 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.661 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.741 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.675 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.619 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.696 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.653 |
MOD_PK_1 | 88 | 94 | PF00069 | 0.532 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.532 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.675 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.598 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.662 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.600 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.685 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.700 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.657 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.567 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.738 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.626 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.741 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.809 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.784 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.639 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.758 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.710 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.562 |
TRG_NES_CRM1_1 | 254 | 268 | PF08389 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V3 | Leptomonas seymouri | 40% | 92% |
A0A3Q8ISN5 | Leishmania donovani | 99% | 100% |
E9B1X6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q686 | Leishmania major | 87% | 100% |