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 |
Related structures:
AlphaFold database: A4I9L2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.653 |
CLV_MEL_PAP_1 | 194 | 200 | PF00089 | 0.566 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.765 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.517 |
CLV_Separin_Metazoa | 366 | 370 | PF03568 | 0.522 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.602 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.706 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.542 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 248 | 256 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.590 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 197 | 201 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 395 | 402 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 411 | 418 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 187 | 203 | PF00022 | 0.575 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.567 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.605 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.679 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.489 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.654 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.655 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.345 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.664 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.700 |
LIG_GBD_Chelix_1 | 132 | 140 | PF00786 | 0.455 |
LIG_HP1_1 | 196 | 200 | PF01393 | 0.579 |
LIG_LIR_Apic_2 | 12 | 17 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 181 | 190 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.603 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.737 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.665 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.744 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.501 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.661 |
LIG_SH3_1 | 168 | 174 | PF00018 | 0.703 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.735 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.777 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.798 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.700 |
LIG_SUMO_SIM_anti_2 | 249 | 255 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 156 | 161 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 352 | 359 | PF11976 | 0.514 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.703 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.679 |
MOD_CDK_SPxK_1 | 67 | 73 | PF00069 | 0.658 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.622 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.732 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.613 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.646 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.718 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.763 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.707 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.614 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.598 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.742 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.558 |
MOD_GlcNHglycan | 50 | 54 | PF01048 | 0.693 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.761 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.695 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.657 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.703 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.520 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.539 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.530 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.640 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.437 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.731 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.524 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.548 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.633 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.594 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.600 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.429 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.556 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.510 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.507 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.508 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.543 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.640 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.594 |
MOD_OFUCOSY | 35 | 40 | PF10250 | 0.638 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.422 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.440 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.545 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.592 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.498 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.599 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.714 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.653 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.643 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.723 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.527 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.679 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.489 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.701 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.686 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.749 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.673 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.822 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.638 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.584 |
MOD_SUMO_rev_2 | 274 | 283 | PF00179 | 0.725 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 198 | 203 | PF01217 | 0.596 |
TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.517 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.731 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW8 | Leptomonas seymouri | 39% | 72% |
A0A3S7X7D6 | Leishmania donovani | 99% | 100% |
A4HAF6 | Leishmania braziliensis | 70% | 98% |
E9B4L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3G6 | Leishmania major | 91% | 100% |