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: A4HBQ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.355 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.322 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.421 |
CLV_Separin_Metazoa | 11 | 15 | PF03568 | 0.464 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.535 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.510 |
DOC_CKS1_1 | 407 | 412 | PF01111 | 0.572 |
DOC_CKS1_1 | 441 | 446 | PF01111 | 0.429 |
DOC_MAPK_gen_1 | 433 | 441 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 433 | 441 | PF00069 | 0.366 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 331 | 339 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 44 | 53 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 89 | 107 | PF00022 | 0.311 |
LIG_BIR_III_4 | 335 | 339 | PF00653 | 0.374 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.544 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.569 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.331 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.432 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.422 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.484 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.563 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.566 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.499 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.409 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.407 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.556 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.626 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 269 | 277 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.359 |
LIG_NRBOX | 357 | 363 | PF00104 | 0.399 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.453 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.552 |
LIG_Pex14_2 | 34 | 38 | PF04695 | 0.335 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.330 |
LIG_SH3_2 | 407 | 412 | PF14604 | 0.415 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.517 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.684 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 236 | 242 | PF11976 | 0.386 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.560 |
LIG_TRAF2_1 | 395 | 398 | PF00917 | 0.550 |
LIG_TYR_ITSM | 139 | 146 | PF00017 | 0.513 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.380 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.425 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.503 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.492 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.469 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.429 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.658 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.489 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.492 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.502 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.573 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.481 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.417 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.395 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.557 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.624 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.500 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.636 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.484 |
MOD_GlcNHglycan | 397 | 402 | PF01048 | 0.554 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.441 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.484 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.501 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.340 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.619 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.438 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.624 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.606 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.487 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.336 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.356 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.361 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.533 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.436 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.325 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.308 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.470 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.614 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.353 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.480 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.381 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.373 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.672 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.502 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.607 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.599 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.463 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.619 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.650 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.431 |
MOD_SUMO_rev_2 | 291 | 300 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 349 | 357 | PF00179 | 0.363 |
TRG_DiLeu_BaEn_1 | 11 | 16 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 296 | 301 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.523 |
TRG_DiLeu_LyEn_5 | 11 | 16 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM65 | Leptomonas seymouri | 38% | 74% |
A0A3S7WWF0 | Leishmania donovani | 76% | 84% |
A4HZ59 | Leishmania infantum | 75% | 84% |
E9AV27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QCF5 | Leishmania major | 75% | 100% |