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: 2, no: 9 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HD09
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.341 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.651 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.563 |
DEG_APCC_DBOX_1 | 397 | 405 | PF00400 | 0.553 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.678 |
DOC_MAPK_gen_1 | 334 | 342 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.711 |
DOC_PP1_RVXF_1 | 366 | 372 | PF00149 | 0.719 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.644 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.646 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.444 |
DOC_USP7_UBL2_3 | 121 | 125 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 368 | 372 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.483 |
LIG_Actin_WH2_2 | 395 | 412 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 316 | 321 | PF00400 | 0.672 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.649 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.390 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.429 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.431 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.582 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.608 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.724 |
LIG_LIR_Apic_2 | 255 | 259 | PF02991 | 0.701 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.716 |
LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 386 | 394 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 370 | 374 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.401 |
LIG_MLH1_MIPbox_1 | 248 | 252 | PF16413 | 0.649 |
LIG_NBox_RRM_1 | 215 | 225 | PF00076 | 0.449 |
LIG_Pex14_2 | 252 | 256 | PF04695 | 0.681 |
LIG_SH2_GRB2like | 272 | 275 | PF00017 | 0.718 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.670 |
LIG_SH2_STAT3 | 288 | 291 | PF00017 | 0.717 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.421 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.419 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.604 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.719 |
LIG_SH3_5 | 264 | 268 | PF00018 | 0.633 |
LIG_SUMO_SIM_par_1 | 10 | 19 | PF11976 | 0.223 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.468 |
LIG_UBA3_1 | 253 | 260 | PF00899 | 0.548 |
LIG_UBA3_1 | 54 | 62 | PF00899 | 0.677 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.602 |
MOD_CDK_SPxxK_3 | 351 | 358 | PF00069 | 0.530 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.294 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.734 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.717 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.595 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.726 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.689 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.549 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.326 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.553 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.716 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.675 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.650 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.419 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.576 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.740 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.630 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.618 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.695 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.557 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.563 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.575 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.547 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.522 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.598 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.612 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.376 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.543 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.645 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.666 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.562 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.561 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.777 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.602 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.570 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.599 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.561 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.466 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.598 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.444 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.649 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.664 |
MOD_Plk_2-3 | 367 | 373 | PF00069 | 0.662 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.531 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.413 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.568 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.724 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.638 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.609 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.533 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.743 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 113 | 123 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 278 | 285 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 326 | 335 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_4 | 132 | 138 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_4 | 311 | 317 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.498 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.698 |
TRG_NES_CRM1_1 | 132 | 144 | PF08389 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S8 | Leptomonas seymouri | 65% | 98% |
A0A0S4IRC9 | Bodo saltans | 34% | 100% |
A0A1X0NWQ4 | Trypanosomatidae | 47% | 97% |
A0A3Q8IMB7 | Leishmania donovani | 78% | 100% |
A0A422NXY7 | Trypanosoma rangeli | 43% | 100% |
A4I0J5 | Leishmania infantum | 78% | 100% |
C9ZVC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AWF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QB16 | Leishmania major | 77% | 100% |
V5BJ93 | Trypanosoma cruzi | 42% | 98% |