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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AYX1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.677 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.669 |
CLV_PCSK_PC7_1 | 306 | 312 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.403 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.836 |
DEG_SCF_FBW7_1 | 140 | 146 | PF00400 | 0.810 |
DEG_SCF_FBW7_1 | 25 | 31 | PF00400 | 0.693 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.681 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.709 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.702 |
DOC_CYCLIN_RxL_1 | 306 | 315 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 347 | 355 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.423 |
DOC_PP1_RVXF_1 | 308 | 315 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.823 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 374 | 381 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 390 | 399 | PF00244 | 0.555 |
LIG_Clathr_ClatBox_1 | 84 | 88 | PF01394 | 0.794 |
LIG_EVH1_2 | 441 | 445 | PF00568 | 0.704 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.613 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.653 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.460 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.481 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.736 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.703 |
LIG_GSK3_LRP6_1 | 37 | 42 | PF00069 | 0.703 |
LIG_IBAR_NPY_1 | 125 | 127 | PF08397 | 0.676 |
LIG_LIR_Apic_2 | 104 | 109 | PF02991 | 0.684 |
LIG_LIR_Apic_2 | 189 | 195 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.599 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.553 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.801 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.682 |
LIG_SH2_PTP2 | 334 | 337 | PF00017 | 0.595 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.809 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 430 | 434 | PF00017 | 0.802 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.697 |
LIG_SH2_STAT3 | 440 | 443 | PF00017 | 0.701 |
LIG_SH2_STAT3 | 8 | 11 | PF00017 | 0.731 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.713 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.493 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.630 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.540 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.669 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.681 |
LIG_SUMO_SIM_anti_2 | 301 | 307 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 83 | 90 | PF11976 | 0.689 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.817 |
LIG_TRAF2_2 | 52 | 57 | PF00917 | 0.706 |
LIG_TRFH_1 | 192 | 196 | PF08558 | 0.513 |
MOD_CDC14_SPxK_1 | 90 | 93 | PF00782 | 0.773 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.776 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.691 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.707 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.709 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.803 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.525 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.729 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.724 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.776 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.698 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.601 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.471 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.475 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.479 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.819 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.532 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.708 |
MOD_Cter_Amidation | 366 | 369 | PF01082 | 0.777 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.718 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.465 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.738 |
MOD_GlcNHglycan | 153 | 157 | PF01048 | 0.688 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.586 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.688 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.695 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.720 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.702 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.677 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.574 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.658 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.696 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.774 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.716 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.703 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.724 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.619 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.748 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.569 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.457 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.695 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.430 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.823 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.497 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.816 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.585 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.577 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.802 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.796 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.740 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.657 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.715 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.644 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.687 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.670 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.497 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.418 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.750 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.624 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.779 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.699 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.794 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.687 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.493 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.593 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.608 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.469 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.724 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.738 |
MOD_Plk_2-3 | 327 | 333 | PF00069 | 0.290 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.436 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.493 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.724 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.693 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.693 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.713 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.485 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.712 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.536 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.590 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.674 |
MOD_SUMO_rev_2 | 351 | 360 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 268 | 273 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 337 | 342 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 311 | 315 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.730 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5L6 | Leptomonas seymouri | 58% | 100% |
A0A3S7X0I2 | Leishmania donovani | 94% | 100% |
A4HFJ4 | Leishmania braziliensis | 73% | 100% |
E9AD47 | Leishmania major | 91% | 100% |
E9AHE1 | Leishmania infantum | 92% | 100% |