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: A4I2B0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.692 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.659 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.583 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.667 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.579 |
CLV_PCSK_PC7_1 | 311 | 317 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.558 |
DEG_SCF_TRCP1_1 | 253 | 258 | PF00400 | 0.611 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.632 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.618 |
DOC_CYCLIN_RxL_1 | 207 | 217 | PF00134 | 0.568 |
DOC_CYCLIN_RxL_1 | 218 | 226 | PF00134 | 0.478 |
DOC_PP1_RVXF_1 | 219 | 226 | PF00149 | 0.595 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.526 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 210 | 220 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.644 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.707 |
LIG_BIR_III_4 | 83 | 87 | PF00653 | 0.636 |
LIG_Clathr_ClatBox_1 | 222 | 226 | PF01394 | 0.555 |
LIG_CSL_BTD_1 | 191 | 194 | PF09270 | 0.599 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.645 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.603 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.697 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.683 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.628 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.680 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.632 |
LIG_PDZ_Class_3 | 376 | 381 | PF00595 | 0.646 |
LIG_Rb_LxCxE_1 | 174 | 190 | PF01857 | 0.658 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 340 | 344 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.601 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.580 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.687 |
LIG_TRFH_1 | 340 | 344 | PF08558 | 0.545 |
LIG_WW_3 | 15 | 19 | PF00397 | 0.583 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.720 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.720 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.519 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.728 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.649 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.609 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.636 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.527 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.682 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.640 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.724 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.612 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.602 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.660 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.558 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.716 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.673 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.710 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.693 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.565 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.675 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.621 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.667 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.579 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.581 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.467 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.551 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.544 |
MOD_GlcNHglycan | 83 | 87 | PF01048 | 0.712 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.643 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.604 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.516 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.586 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.643 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.698 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.597 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.434 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.414 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.637 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.628 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.593 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.713 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.688 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.707 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.615 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.637 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.645 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.607 |
MOD_PK_1 | 100 | 106 | PF00069 | 0.572 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.576 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.651 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.663 |
MOD_PKB_1 | 315 | 323 | PF00069 | 0.665 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.664 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.637 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.600 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.586 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.650 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.576 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.720 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.697 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.575 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.570 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.623 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.547 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICW3 | Leishmania donovani | 99% | 100% |
E9AIQ9 | Leishmania braziliensis | 65% | 100% |
E9AYF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q915 | Leishmania major | 88% | 100% |