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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B224
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.663 |
CLV_PCSK_FUR_1 | 245 | 249 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.622 |
DOC_CDC14_PxL_1 | 38 | 46 | PF14671 | 0.589 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.507 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.580 |
DOC_PP1_RVXF_1 | 365 | 372 | PF00149 | 0.587 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.493 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 37 | 42 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 403 | 412 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.594 |
LIG_BIR_III_4 | 92 | 96 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.587 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.613 |
LIG_deltaCOP1_diTrp_1 | 363 | 371 | PF00928 | 0.512 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.570 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.699 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.621 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.775 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.587 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.581 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.645 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.506 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.718 |
LIG_LIR_Gen_1 | 137 | 148 | PF02991 | 0.671 |
LIG_LIR_LC3C_4 | 56 | 61 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.578 |
LIG_NRBOX | 328 | 334 | PF00104 | 0.502 |
LIG_Pex14_1 | 155 | 159 | PF04695 | 0.616 |
LIG_SH2_NCK_1 | 38 | 42 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 49 | 53 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.619 |
LIG_SH3_2 | 64 | 69 | PF14604 | 0.696 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.702 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.718 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.697 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.535 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.644 |
LIG_SUMO_SIM_anti_2 | 56 | 63 | PF11976 | 0.617 |
LIG_SUMO_SIM_par_1 | 56 | 63 | PF11976 | 0.623 |
LIG_WW_3 | 386 | 390 | PF00397 | 0.506 |
LIG_WW_3 | 437 | 441 | PF00397 | 0.759 |
MOD_CDC14_SPxK_1 | 386 | 389 | PF00782 | 0.599 |
MOD_CDC14_SPxK_1 | 66 | 69 | PF00782 | 0.698 |
MOD_CDK_SPK_2 | 191 | 196 | PF00069 | 0.709 |
MOD_CDK_SPK_2 | 63 | 68 | PF00069 | 0.521 |
MOD_CDK_SPxK_1 | 383 | 389 | PF00069 | 0.599 |
MOD_CDK_SPxK_1 | 63 | 69 | PF00069 | 0.698 |
MOD_CDK_SPxxK_3 | 321 | 328 | PF00069 | 0.505 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.803 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.673 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.662 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.665 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.530 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.651 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.574 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.672 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.809 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.690 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.714 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.651 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.570 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.670 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.506 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.715 |
MOD_Cter_Amidation | 232 | 235 | PF01082 | 0.566 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.766 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.722 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.780 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.708 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.633 |
MOD_GlcNHglycan | 28 | 32 | PF01048 | 0.678 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.654 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.620 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.566 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.711 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.543 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.572 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.584 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.614 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.575 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.661 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.570 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.669 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.708 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.665 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.676 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.641 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.687 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.607 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.701 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.769 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.680 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.780 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.553 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.596 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.691 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.708 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.539 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.589 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.666 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.542 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.643 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.717 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.617 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.760 |
MOD_PKB_1 | 401 | 409 | PF00069 | 0.724 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.691 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.609 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.642 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.586 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.556 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.536 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.596 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.719 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.506 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.752 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.608 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.638 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.694 |
TRG_AP2beta_CARGO_1 | 138 | 147 | PF09066 | 0.664 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.508 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 439 | 442 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ50 | Leptomonas seymouri | 36% | 98% |
A0A3S7X4S8 | Leishmania donovani | 76% | 100% |
A4HJK4 | Leishmania braziliensis | 52% | 99% |
A4HJK7 | Leishmania braziliensis | 52% | 99% |
A4I706 | Leishmania infantum | 76% | 100% |
Q4Q638 | Leishmania major | 74% | 100% |