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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4I817
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.644 |
CLV_PCSK_FUR_1 | 417 | 421 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.584 |
DEG_COP1_1 | 170 | 179 | PF00400 | 0.570 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.623 |
DEG_SCF_TRCP1_1 | 468 | 474 | PF00400 | 0.588 |
DEG_SIAH_1 | 402 | 410 | PF03145 | 0.561 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.553 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.687 |
DOC_CYCLIN_RxL_1 | 385 | 397 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 262 | 270 | PF00069 | 0.692 |
DOC_MAPK_RevD_3 | 405 | 420 | PF00069 | 0.611 |
DOC_PP4_FxxP_1 | 275 | 278 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 262 | 270 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 338 | 348 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.565 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.627 |
LIG_CaM_IQ_9 | 439 | 455 | PF13499 | 0.589 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.609 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.644 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.699 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.516 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.682 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.594 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.673 |
LIG_GBD_Chelix_1 | 344 | 352 | PF00786 | 0.560 |
LIG_IRF3_LxIS_1 | 348 | 355 | PF10401 | 0.583 |
LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 136 | 147 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.752 |
LIG_LYPXL_yS_3 | 132 | 135 | PF13949 | 0.598 |
LIG_MYND_1 | 173 | 177 | PF01753 | 0.629 |
LIG_PCNA_yPIPBox_3 | 338 | 348 | PF02747 | 0.512 |
LIG_PDZ_Class_1 | 471 | 476 | PF00595 | 0.591 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.658 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.632 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.772 |
LIG_SUMO_SIM_par_1 | 170 | 178 | PF11976 | 0.605 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.674 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.670 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.544 |
LIG_TYR_ITIM | 130 | 135 | PF00017 | 0.603 |
LIG_UBA3_1 | 17 | 23 | PF00899 | 0.537 |
LIG_WRC_WIRS_1 | 207 | 212 | PF05994 | 0.582 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.660 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.661 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.680 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.702 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.602 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.673 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.583 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.619 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.635 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.717 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.693 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.643 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.568 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.695 |
MOD_Cter_Amidation | 382 | 385 | PF01082 | 0.654 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.654 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.447 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.672 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.685 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.677 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.678 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.658 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.658 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.528 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.584 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.608 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.758 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.628 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.576 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.656 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.521 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.607 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.689 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.661 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.640 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.600 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.500 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.656 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.549 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.672 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.563 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.609 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.653 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.523 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.633 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.737 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.615 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.659 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.525 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.547 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.652 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.581 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.634 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.651 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.654 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.701 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.661 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.568 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.532 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.620 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.607 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.687 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.632 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.550 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.669 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.575 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.634 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.611 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.627 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.615 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.654 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.609 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.766 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.613 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.627 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.628 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.633 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.620 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.630 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.639 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.602 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.668 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.689 |
MOD_SUMO_rev_2 | 153 | 159 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 29 | 38 | PF00179 | 0.525 |
TRG_DiLeu_BaEn_1 | 373 | 378 | PF01217 | 0.644 |
TRG_DiLeu_BaEn_1 | 43 | 48 | PF01217 | 0.606 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.562 |
TRG_ER_diArg_1 | 416 | 419 | PF00400 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 391 | 396 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 450 | 454 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5L4 | Leishmania donovani | 98% | 100% |
A4HKI6 | Leishmania braziliensis | 50% | 100% |
E9B2X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q581 | Leishmania major | 83% | 100% |