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: Q4Q1J4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.478 |
DEG_COP1_1 | 229 | 237 | PF00400 | 0.594 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.629 |
DOC_CYCLIN_yCln2_LP_2 | 130 | 136 | PF00134 | 0.601 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.573 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 304 | 312 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 333 | 337 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.386 |
LIG_APCC_ABBA_1 | 436 | 441 | PF00400 | 0.467 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.513 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.513 |
LIG_CaM_IQ_9 | 55 | 70 | PF13499 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 350 | 356 | PF00928 | 0.526 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.605 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.624 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.512 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.581 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.505 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.428 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.586 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.632 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.654 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.617 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.449 |
LIG_LIR_Gen_1 | 125 | 136 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 350 | 360 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 437 | 447 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 60 | 67 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 73 | 84 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.505 |
LIG_PCNA_yPIPBox_3 | 450 | 459 | PF02747 | 0.457 |
LIG_PCNA_yPIPBox_3 | 63 | 75 | PF02747 | 0.475 |
LIG_PDZ_Class_2 | 456 | 461 | PF00595 | 0.562 |
LIG_Pex14_1 | 274 | 278 | PF04695 | 0.552 |
LIG_Rb_pABgroove_1 | 111 | 119 | PF01858 | 0.359 |
LIG_RPA_C_Fungi | 29 | 41 | PF08784 | 0.495 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.588 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.502 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.571 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.567 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.527 |
LIG_SUMO_SIM_par_1 | 134 | 139 | PF11976 | 0.632 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.589 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.527 |
LIG_WRC_WIRS_1 | 244 | 249 | PF05994 | 0.528 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.594 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.681 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.475 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.764 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.665 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.510 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.647 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.626 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.666 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.507 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.513 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.567 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.506 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.561 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.400 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.606 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.787 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.660 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.421 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.623 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.598 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.477 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.572 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.493 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.648 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.765 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.728 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.713 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.641 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.574 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.567 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.605 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.551 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.636 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.740 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.603 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.633 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.451 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.560 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.466 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.600 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.629 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.507 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.636 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.596 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.444 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.388 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.629 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.558 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.559 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.668 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.549 |
MOD_SUMO_rev_2 | 215 | 223 | PF00179 | 0.642 |
TRG_DiLeu_BaEn_4 | 331 | 337 | PF01217 | 0.594 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAU2 | Leishmania donovani | 90% | 100% |
A4HP96 | Leishmania braziliensis | 69% | 99% |
A4IDK1 | Leishmania infantum | 90% | 100% |
E9AT04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |