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: A4I706
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.726 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.823 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.612 |
CLV_PCSK_FUR_1 | 245 | 249 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.740 |
CLV_Separin_Metazoa | 339 | 343 | PF03568 | 0.585 |
DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.578 |
DOC_CDC14_PxL_1 | 38 | 46 | PF14671 | 0.705 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.776 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 281 | 291 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 37 | 42 | PF00244 | 0.705 |
LIG_BIR_III_2 | 62 | 66 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.594 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.660 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.651 |
LIG_eIF4E_1 | 38 | 44 | PF01652 | 0.577 |
LIG_eIF4E_1 | 71 | 77 | PF01652 | 0.687 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.711 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.643 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.639 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.615 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.718 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.693 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.649 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.694 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.671 |
LIG_LIR_Gen_1 | 268 | 279 | PF02991 | 0.688 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.806 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.797 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.602 |
LIG_PAM2_1 | 15 | 27 | PF00658 | 0.686 |
LIG_Pex14_1 | 155 | 159 | PF04695 | 0.780 |
LIG_SH2_NCK_1 | 38 | 42 | PF00017 | 0.728 |
LIG_SH2_NCK_1 | 49 | 53 | PF00017 | 0.624 |
LIG_SH2_PTP2 | 71 | 74 | PF00017 | 0.604 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.684 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.766 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.684 |
LIG_SH3_2 | 380 | 385 | PF14604 | 0.583 |
LIG_SH3_2 | 64 | 69 | PF14604 | 0.720 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.665 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.728 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.734 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.730 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.574 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.780 |
LIG_WW_3 | 433 | 437 | PF00397 | 0.748 |
MOD_CDC14_SPxK_1 | 382 | 385 | PF00782 | 0.626 |
MOD_CDC14_SPxK_1 | 66 | 69 | PF00782 | 0.703 |
MOD_CDK_SPK_2 | 191 | 196 | PF00069 | 0.739 |
MOD_CDK_SPxK_1 | 379 | 385 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.704 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.673 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.656 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.838 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.696 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.702 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.638 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.802 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.766 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.571 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.796 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.672 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.738 |
MOD_Cter_Amidation | 279 | 282 | PF01082 | 0.611 |
MOD_DYRK1A_RPxSP_1 | 379 | 383 | PF00069 | 0.576 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.707 |
MOD_GlcNHglycan | 127 | 131 | PF01048 | 0.716 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.716 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.711 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.606 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.723 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.737 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.692 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.661 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.678 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.818 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.646 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.688 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.604 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.791 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.789 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.527 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.764 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.678 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.714 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.660 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.655 |
MOD_N-GLC_2 | 406 | 408 | PF02516 | 0.627 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.776 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.682 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.794 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.764 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.717 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.736 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.653 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.781 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.785 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.780 |
MOD_PKB_1 | 397 | 405 | PF00069 | 0.732 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.700 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.699 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.682 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.785 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.748 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.736 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.785 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.636 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.681 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.737 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.777 |
MOD_SUMO_rev_2 | 345 | 350 | PF00179 | 0.766 |
TRG_AP2beta_CARGO_1 | 138 | 147 | PF09066 | 0.668 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.656 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.748 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4S8 | Leishmania donovani | 98% | 100% |
A4HJK4 | Leishmania braziliensis | 53% | 100% |
A4HJK7 | Leishmania braziliensis | 52% | 100% |
E9B224 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q638 | Leishmania major | 82% | 100% |