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: A4IDK1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.770 |
CLV_MEL_PAP_1 | 78 | 84 | PF00089 | 0.407 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.768 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.513 |
CLV_Separin_Metazoa | 69 | 73 | PF03568 | 0.532 |
DEG_APCC_DBOX_1 | 71 | 79 | PF00400 | 0.432 |
DEG_COP1_1 | 229 | 237 | PF00400 | 0.684 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.731 |
DOC_CYCLIN_yCln2_LP_2 | 130 | 136 | PF00134 | 0.710 |
DOC_MAPK_MEF2A_6 | 59 | 66 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.575 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.865 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 304 | 312 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 394 | 398 | PF00244 | 0.637 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.649 |
LIG_deltaCOP1_diTrp_1 | 350 | 356 | PF00928 | 0.652 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.645 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.485 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.714 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.708 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.523 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.729 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.733 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.663 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.764 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.553 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.552 |
LIG_GBD_Chelix_1 | 66 | 74 | PF00786 | 0.434 |
LIG_LIR_Gen_1 | 125 | 136 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 350 | 360 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 386 | 393 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 437 | 447 | PF02991 | 0.727 |
LIG_LIR_Gen_1 | 60 | 67 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 73 | 84 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.728 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.625 |
LIG_PCNA_yPIPBox_3 | 63 | 75 | PF02747 | 0.616 |
LIG_Pex14_1 | 274 | 278 | PF04695 | 0.541 |
LIG_RPA_C_Fungi | 29 | 41 | PF08784 | 0.632 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.718 |
LIG_SH2_PTP2 | 389 | 392 | PF00017 | 0.526 |
LIG_SH2_PTP2 | 458 | 461 | PF00017 | 0.542 |
LIG_SH2_SRC | 439 | 442 | PF00017 | 0.641 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.677 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.751 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.618 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.584 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.716 |
LIG_SUMO_SIM_par_1 | 134 | 139 | PF11976 | 0.759 |
LIG_SUMO_SIM_par_1 | 50 | 55 | PF11976 | 0.368 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.718 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.675 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.634 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.827 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.615 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.728 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.700 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.686 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.778 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.559 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.745 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.767 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.795 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.625 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.625 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.665 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.711 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.678 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.481 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.588 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.554 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.771 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.683 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.595 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.636 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.573 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.779 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.622 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.790 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.796 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.672 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.760 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.676 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.702 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.609 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.765 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.757 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.653 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.696 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.619 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.621 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.582 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.670 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.379 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.690 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.718 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.638 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.423 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.442 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.540 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.443 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.480 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.592 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.754 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.578 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.752 |
MOD_SUMO_rev_2 | 215 | 223 | PF00179 | 0.743 |
TRG_DiLeu_BaEn_4 | 331 | 337 | PF01217 | 0.703 |
TRG_DiLeu_BaLyEn_6 | 366 | 371 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.675 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.719 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAU2 | Leishmania donovani | 100% | 100% |
A4HP96 | Leishmania braziliensis | 71% | 100% |
E9AT04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q1J4 | Leishmania major | 90% | 100% |