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: A0A3Q8I7N0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.450 |
CLV_PCSK_FUR_1 | 419 | 423 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.796 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.629 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.515 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.604 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.705 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.575 |
DOC_MAPK_MEF2A_6 | 295 | 304 | PF00069 | 0.611 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 114 | 118 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 22 | 32 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 323 | 333 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 369 | 374 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 384 | 391 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 131 | 149 | PF00022 | 0.583 |
LIG_Actin_WH2_2 | 315 | 332 | PF00022 | 0.642 |
LIG_BIR_III_2 | 206 | 210 | PF00653 | 0.626 |
LIG_CaM_IQ_9 | 361 | 377 | PF13499 | 0.454 |
LIG_DLG_GKlike_1 | 369 | 377 | PF00625 | 0.462 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.562 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.462 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.657 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.532 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.691 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.563 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.640 |
LIG_GBD_Chelix_1 | 290 | 298 | PF00786 | 0.597 |
LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.536 |
LIG_PROFILIN_1 | 403 | 409 | PF00235 | 0.579 |
LIG_RPA_C_Fungi | 379 | 391 | PF08784 | 0.503 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.462 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.657 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.697 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.657 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.726 |
LIG_SUMO_SIM_anti_2 | 317 | 324 | PF11976 | 0.643 |
LIG_SUMO_SIM_par_1 | 160 | 166 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.498 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.691 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.631 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.622 |
MOD_CDK_SPK_2 | 394 | 399 | PF00069 | 0.753 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.525 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.521 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.616 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.573 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.703 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.630 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.648 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.696 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.720 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.641 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.680 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.690 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.610 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.669 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.584 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.675 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.574 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.551 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.695 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.587 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.637 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.539 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.591 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.649 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.634 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.599 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.699 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.616 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.598 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.627 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.745 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.558 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.402 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.546 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.541 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.615 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.424 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.563 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.572 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.697 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.561 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.652 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.525 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.680 |
MOD_PK_1 | 147 | 153 | PF00069 | 0.511 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.498 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.525 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.539 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.583 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.505 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.696 |
MOD_PKB_1 | 369 | 377 | PF00069 | 0.462 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.400 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.573 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.511 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.639 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.583 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.788 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.475 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.462 |
TRG_NES_CRM1_1 | 288 | 303 | PF08389 | 0.544 |
TRG_NES_CRM1_1 | 354 | 365 | PF08389 | 0.626 |
TRG_NLS_MonoExtC_3 | 121 | 127 | PF00514 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC0 | Leptomonas seymouri | 36% | 80% |
A4H616 | Leishmania braziliensis | 69% | 100% |
A4HUE3 | Leishmania infantum | 99% | 100% |
E9AN43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHI3 | Leishmania major | 91% | 100% |