Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A4HJ56
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.364 |
CLV_MEL_PAP_1 | 284 | 290 | PF00089 | 0.533 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.490 |
CLV_Separin_Metazoa | 74 | 78 | PF03568 | 0.278 |
DOC_CKS1_1 | 59 | 64 | PF01111 | 0.324 |
DOC_MAPK_gen_1 | 122 | 130 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 279 | 286 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 354 | 361 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 77 | 84 | PF00069 | 0.296 |
DOC_MAPK_JIP1_4 | 280 | 286 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.536 |
DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.534 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.322 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 315 | 320 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 387 | 397 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 88 | 105 | PF00022 | 0.428 |
LIG_AP2alpha_1 | 171 | 175 | PF02296 | 0.397 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.565 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_2 | 274 | 280 | PF00533 | 0.535 |
LIG_Clathr_ClatBox_1 | 96 | 100 | PF01394 | 0.292 |
LIG_DLG_GKlike_1 | 157 | 164 | PF00625 | 0.330 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.312 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.406 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.594 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.649 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.462 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.323 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.446 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.400 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.458 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.530 |
LIG_Integrin_isoDGR_2 | 259 | 261 | PF01839 | 0.535 |
LIG_LIR_Apic_2 | 275 | 281 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 56 | 62 | PF02991 | 0.333 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.428 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.420 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.344 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.382 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.660 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.501 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.759 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.546 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.380 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.453 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.380 |
LIG_TRFH_1 | 254 | 258 | PF08558 | 0.615 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.400 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.376 |
LIG_WRC_WIRS_1 | 382 | 387 | PF05994 | 0.564 |
LIG_WW_1 | 380 | 383 | PF00397 | 0.553 |
MOD_CDC14_SPxK_1 | 312 | 315 | PF00782 | 0.560 |
MOD_CDK_SPK_2 | 261 | 266 | PF00069 | 0.540 |
MOD_CDK_SPxK_1 | 309 | 315 | PF00069 | 0.565 |
MOD_CDK_SPxxK_3 | 58 | 65 | PF00069 | 0.329 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.548 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.418 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.508 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.321 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.546 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.517 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.539 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.571 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.371 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.587 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.336 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.410 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.317 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.434 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.394 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.453 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.525 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.542 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.416 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.411 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.501 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.587 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.300 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.380 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.751 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.716 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.787 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.553 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.550 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.520 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.566 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.506 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.414 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.386 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.540 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.555 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.433 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.390 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.465 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.319 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.378 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.562 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.593 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.433 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.412 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.534 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.548 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.560 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.515 |
MOD_PK_1 | 315 | 321 | PF00069 | 0.539 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.434 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.585 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.538 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.564 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.312 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.354 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.439 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.512 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.425 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.513 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.405 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.434 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.675 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.615 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.679 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.544 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.517 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.340 |
MOD_SUMO_for_1 | 113 | 116 | PF00179 | 0.403 |
MOD_SUMO_rev_2 | 167 | 176 | PF00179 | 0.307 |
MOD_SUMO_rev_2 | 413 | 423 | PF00179 | 0.436 |
TRG_DiLeu_BaEn_1 | 348 | 353 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 216 | 222 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.530 |
TRG_NLS_MonoExtN_4 | 122 | 128 | PF00514 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3S1 | Leptomonas seymouri | 58% | 95% |
A0A3Q8IG21 | Leishmania donovani | 66% | 100% |
A0A3Q8IIE7 | Leishmania donovani | 66% | 100% |
A4H6C6 | Leishmania braziliensis | 21% | 100% |
A4I6H9 | Leishmania infantum | 66% | 100% |
E9AHL0 | Leishmania infantum | 68% | 100% |
E9B1M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9B1N5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9B1N6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
Q4Q6H8 | Leishmania major | 64% | 100% |
Q4Q6I6 | Leishmania major | 69% | 100% |
Q4QI82 | Leishmania major | 24% | 100% |