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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9ACL8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.600 |
CLV_PCSK_FUR_1 | 297 | 301 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.632 |
CLV_Separin_Metazoa | 125 | 129 | PF03568 | 0.592 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.733 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.627 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.750 |
DOC_MAPK_gen_1 | 217 | 225 | PF00069 | 0.647 |
DOC_MAPK_MEF2A_6 | 200 | 209 | PF00069 | 0.516 |
DOC_MAPK_NFAT4_5 | 206 | 214 | PF00069 | 0.459 |
DOC_MAPK_RevD_3 | 203 | 218 | PF00069 | 0.537 |
DOC_PP2B_LxvP_1 | 136 | 139 | PF13499 | 0.781 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.644 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.697 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.794 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.589 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 200 | 207 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 248 | 255 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.713 |
LIG_Actin_WH2_1 | 206 | 223 | PF00022 | 0.549 |
LIG_Actin_WH2_2 | 207 | 223 | PF00022 | 0.548 |
LIG_APCC_ABBA_1 | 53 | 58 | PF00400 | 0.593 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BIR_III_2 | 166 | 170 | PF00653 | 0.622 |
LIG_BIR_III_2 | 346 | 350 | PF00653 | 0.627 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.684 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.573 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.593 |
LIG_deltaCOP1_diTrp_1 | 166 | 171 | PF00928 | 0.668 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.670 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.586 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.550 |
LIG_LIR_Apic_2 | 170 | 174 | PF02991 | 0.713 |
LIG_LIR_Apic_2 | 367 | 373 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.594 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 374 | 377 | PF00017 | 0.716 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.619 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.563 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.579 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.694 |
LIG_TRAF2_1 | 306 | 309 | PF00917 | 0.615 |
MOD_CDC14_SPxK_1 | 350 | 353 | PF00782 | 0.615 |
MOD_CDK_SPxK_1 | 145 | 151 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 347 | 353 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 391 | 397 | PF00069 | 0.707 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.657 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.535 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.535 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.671 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.563 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.589 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.659 |
MOD_CMANNOS | 168 | 171 | PF00535 | 0.663 |
MOD_Cter_Amidation | 23 | 26 | PF01082 | 0.692 |
MOD_Cter_Amidation | 92 | 95 | PF01082 | 0.389 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.625 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.596 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.527 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.665 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.685 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.483 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.630 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.719 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.626 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.644 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.612 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.641 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.607 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.666 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.683 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.612 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.608 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.418 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.518 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.684 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.651 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.622 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.718 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.640 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.722 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.686 |
MOD_PKA_1 | 155 | 161 | PF00069 | 0.654 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.768 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.664 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.631 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.460 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.664 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.768 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.535 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.656 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.608 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.554 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.525 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.475 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.750 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.616 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.634 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.735 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.746 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.754 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 152 | 157 | PF00179 | 0.670 |
TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.676 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.624 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.683 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 257 | 271 | PF08389 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 162 | 166 | PF00026 | 0.693 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBW0 | Leptomonas seymouri | 40% | 84% |
A0A3R7KL86 | Trypanosoma rangeli | 23% | 100% |
A0A451EJS2 | Leishmania donovani | 91% | 99% |
A4H3N4 | Leishmania braziliensis | 61% | 73% |
A4HRW1 | Leishmania infantum | 91% | 99% |
E9AJV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |