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: Q4Q4A5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.677 |
CLV_MEL_PAP_1 | 259 | 265 | PF00089 | 0.525 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.637 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.401 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.679 |
DOC_CYCLIN_RxL_1 | 203 | 210 | PF00134 | 0.416 |
DOC_CYCLIN_RxL_1 | 474 | 485 | PF00134 | 0.462 |
DOC_MAPK_MEF2A_6 | 198 | 205 | PF00069 | 0.326 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 477 | 484 | PF00149 | 0.492 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.390 |
DOC_PP4_FxxP_1 | 336 | 339 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.627 |
DOC_USP7_UBL2_3 | 56 | 60 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.550 |
LIG_Actin_WH2_2 | 266 | 283 | PF00022 | 0.461 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.501 |
LIG_APCC_ABBAyCdc20_2 | 479 | 485 | PF00400 | 0.391 |
LIG_EH_1 | 2 | 6 | PF12763 | 0.530 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.713 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.369 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.697 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.521 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.620 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.536 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.621 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.511 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 424 | 430 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.681 |
LIG_MYND_3 | 429 | 433 | PF01753 | 0.405 |
LIG_Rb_pABgroove_1 | 437 | 445 | PF01858 | 0.489 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.369 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.654 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.489 |
LIG_SH2_GRB2like | 484 | 487 | PF00017 | 0.390 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.489 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.569 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.549 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.616 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.550 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.685 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.587 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.607 |
LIG_SH3_5 | 380 | 384 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 447 | 452 | PF11976 | 0.378 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.719 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.506 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.545 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.649 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.537 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.506 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.564 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.705 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.636 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.629 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.700 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.697 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.526 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.627 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.548 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.531 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.515 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.508 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.551 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.607 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.595 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.572 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.625 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.614 |
MOD_GlcNHglycan | 414 | 418 | PF01048 | 0.730 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.716 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.728 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.641 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.633 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.510 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.754 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.638 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.705 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.566 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.548 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.635 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.424 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.550 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.543 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.648 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.624 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.521 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.410 |
MOD_PK_1 | 435 | 441 | PF00069 | 0.377 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.542 |
MOD_PKA_1 | 453 | 459 | PF00069 | 0.410 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.550 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.662 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.687 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.528 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.575 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.728 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.500 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.494 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.667 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.448 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.389 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.735 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.548 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.519 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.644 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.552 |
MOD_SUMO_for_1 | 324 | 327 | PF00179 | 0.663 |
MOD_SUMO_for_1 | 361 | 364 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 428 | 437 | PF00179 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 427 | 432 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.392 |
TRG_NLS_Bipartite_1 | 40 | 62 | PF00514 | 0.604 |
TRG_NLS_MonoExtC_3 | 118 | 124 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 56 | 62 | PF00514 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBA2 | Leptomonas seymouri | 43% | 100% |
A0A3Q8ITX1 | Leishmania donovani | 93% | 100% |
A4HLE1 | Leishmania braziliensis | 74% | 100% |
A4I8V0 | Leishmania infantum | 93% | 100% |
E9B3R9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |