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: 6 |
NetGPI | no | yes: 0, no: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I4S7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.581 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.671 |
CLV_PCSK_FUR_1 | 441 | 445 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.633 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.589 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.279 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.334 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.512 |
DOC_CYCLIN_RxL_1 | 240 | 251 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.397 |
DOC_MAPK_JIP1_4 | 319 | 325 | PF00069 | 0.279 |
DOC_PP1_RVXF_1 | 417 | 423 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.704 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.279 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.703 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 380 | 387 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.609 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.710 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.597 |
LIG_deltaCOP1_diTrp_1 | 287 | 295 | PF00928 | 0.334 |
LIG_EH_1 | 331 | 335 | PF12763 | 0.279 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.647 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.655 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.512 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.509 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.664 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.596 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.717 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.705 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 397 | 401 | PF02991 | 0.279 |
LIG_MYND_1 | 333 | 337 | PF01753 | 0.279 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 359 | 363 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.466 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.334 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.529 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.772 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.536 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.652 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.557 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.529 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.290 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.442 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.334 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.672 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.606 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.584 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.663 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.625 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.611 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.653 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.486 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.657 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.598 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.279 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.279 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.262 |
MOD_GlcNHglycan | 338 | 343 | PF01048 | 0.253 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.395 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.707 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.695 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.707 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.685 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.583 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.429 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.706 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.706 |
MOD_LATS_1 | 454 | 460 | PF00433 | 0.581 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.528 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.570 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.548 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.420 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.370 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.697 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.713 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.491 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.606 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.593 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.584 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.597 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.616 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.601 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.391 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.243 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.330 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.288 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.658 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.521 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.279 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.599 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.699 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.490 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.279 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.521 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.545 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.397 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.579 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.541 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.540 |
MOD_SUMO_for_1 | 335 | 338 | PF00179 | 0.269 |
MOD_SUMO_rev_2 | 19 | 28 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 409 | 418 | PF00179 | 0.257 |
MOD_SUMO_rev_2 | 79 | 88 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_4 | 390 | 396 | PF01217 | 0.520 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.391 |
TRG_NLS_Bipartite_1 | 86 | 104 | PF00514 | 0.686 |
TRG_NLS_MonoExtN_4 | 97 | 104 | PF00514 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKX8 | Leptomonas seymouri | 52% | 98% |
A0A3Q8IEK2 | Leishmania donovani | 99% | 100% |
A4HHL8 | Leishmania braziliensis | 73% | 100% |
E9AE80 | Leishmania major | 89% | 100% |
E9ALK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |