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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HAE3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.581 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.772 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.597 |
CLV_Separin_Metazoa | 150 | 154 | PF03568 | 0.501 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.654 |
DOC_CKS1_1 | 203 | 208 | PF01111 | 0.511 |
DOC_CKS1_1 | 249 | 254 | PF01111 | 0.546 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.781 |
DOC_USP7_MATH_2 | 2 | 8 | PF00917 | 0.667 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.625 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 349 | 356 | PF00244 | 0.472 |
LIG_Clathr_ClatBox_1 | 295 | 299 | PF01394 | 0.625 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.627 |
LIG_EVH1_1 | 277 | 281 | PF00568 | 0.543 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.617 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.636 |
LIG_HCF-1_HBM_1 | 19 | 22 | PF13415 | 0.504 |
LIG_LIR_Apic_2 | 99 | 104 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 161 | 168 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.648 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.655 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.494 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.666 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.626 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.658 |
LIG_SH3_2 | 249 | 254 | PF14604 | 0.635 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.553 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.568 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.662 |
LIG_SH3_CIN85_PxpxPR_1 | 111 | 116 | PF14604 | 0.653 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.609 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.614 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.545 |
LIG_WW_3 | 222 | 226 | PF00397 | 0.575 |
MOD_CDK_SPxK_1 | 248 | 254 | PF00069 | 0.545 |
MOD_CDK_SPxxK_3 | 100 | 107 | PF00069 | 0.656 |
MOD_CDK_SPxxK_3 | 109 | 116 | PF00069 | 0.690 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.534 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.734 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.510 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.556 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.591 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.665 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.550 |
MOD_Cter_Amidation | 36 | 39 | PF01082 | 0.624 |
MOD_DYRK1A_RPxSP_1 | 244 | 248 | PF00069 | 0.593 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.655 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.743 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.558 |
MOD_GlcNHglycan | 4 | 9 | PF01048 | 0.752 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.573 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.497 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.709 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.659 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.713 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.511 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.655 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.628 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.629 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.735 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.574 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.423 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.454 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.624 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.663 |
MOD_PK_1 | 81 | 87 | PF00069 | 0.541 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.722 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.681 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.527 |
MOD_PKB_1 | 317 | 325 | PF00069 | 0.635 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.375 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.541 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.675 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.376 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.485 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.627 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.652 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.636 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.629 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.595 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.504 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.686 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.621 |
MOD_SUMO_for_1 | 140 | 143 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 163 | 172 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 50 | 56 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.619 |
TRG_DiLeu_BaEn_2 | 91 | 97 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.710 |
TRG_NLS_Bipartite_1 | 301 | 320 | PF00514 | 0.585 |
TRG_NLS_MonoExtC_3 | 137 | 143 | PF00514 | 0.486 |
TRG_NLS_MonoExtN_4 | 136 | 142 | PF00514 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 258 | 262 | PF00026 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 370 | 375 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK05 | Leptomonas seymouri | 58% | 92% |
A0A1X0P9W7 | Trypanosomatidae | 37% | 100% |
A0A3R7K419 | Trypanosoma rangeli | 33% | 98% |
A0A3S5H7V7 | Leishmania donovani | 82% | 100% |
A4I9J5 | Leishmania infantum | 82% | 100% |
E9B4J3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q3I3 | Leishmania major | 80% | 100% |
V5B266 | Trypanosoma cruzi | 33% | 100% |