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: E9B318
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.772 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.667 |
CLV_PCSK_FUR_1 | 139 | 143 | PF00082 | 0.749 |
CLV_PCSK_FUR_1 | 65 | 69 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.818 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.726 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.737 |
CLV_Separin_Metazoa | 148 | 152 | PF03568 | 0.685 |
DEG_APCC_DBOX_1 | 464 | 472 | PF00400 | 0.367 |
DEG_Kelch_Keap1_1 | 104 | 109 | PF01344 | 0.727 |
DEG_SCF_FBW7_2 | 171 | 178 | PF00400 | 0.708 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.670 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.785 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.513 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.709 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.782 |
DOC_MAPK_gen_1 | 140 | 152 | PF00069 | 0.704 |
DOC_MAPK_gen_1 | 226 | 232 | PF00069 | 0.790 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.725 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.672 |
DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.822 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.431 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.805 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 236 | 243 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 349 | 357 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 455 | 461 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.620 |
LIG_BIR_III_4 | 130 | 134 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.638 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.653 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.619 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.551 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.791 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.566 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.395 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.618 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.521 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.560 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.804 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 473 | 481 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.541 |
LIG_MLH1_MIPbox_1 | 88 | 92 | PF16413 | 0.638 |
LIG_PCNA_yPIPBox_3 | 321 | 335 | PF02747 | 0.524 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.540 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.576 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.690 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.641 |
LIG_TRAF2_1 | 486 | 489 | PF00917 | 0.573 |
LIG_TYR_ITIM | 152 | 157 | PF00017 | 0.546 |
LIG_WRC_WIRS_1 | 331 | 336 | PF05994 | 0.598 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.558 |
MOD_CDK_SPxK_1 | 262 | 268 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 156 | 163 | PF00069 | 0.511 |
MOD_CDK_SPxxK_3 | 220 | 227 | PF00069 | 0.561 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.776 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.659 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.698 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.689 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.795 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.728 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.655 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.523 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.556 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.543 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.633 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.530 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.658 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.721 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.664 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.700 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.702 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.698 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.719 |
MOD_GlcNHglycan | 374 | 378 | PF01048 | 0.769 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.737 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.720 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.714 |
MOD_GlcNHglycan | 433 | 437 | PF01048 | 0.485 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.366 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.651 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.695 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.637 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.712 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.767 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.689 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.551 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.702 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.632 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.498 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.472 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.444 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.648 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.719 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.737 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.640 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.705 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.584 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.663 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.527 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.613 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.484 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.707 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.597 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.638 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.651 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.323 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.691 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.629 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.585 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.534 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.368 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.627 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.731 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.695 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.664 |
MOD_Plk_2-3 | 273 | 279 | PF00069 | 0.679 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.712 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.535 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.561 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.532 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.584 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.632 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.551 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.766 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.599 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.730 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 270 | 277 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 215 | 220 | PF01217 | 0.704 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.699 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.751 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.733 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.667 |
TRG_NLS_Bipartite_1 | 122 | 144 | PF00514 | 0.742 |
TRG_NLS_MonoCore_2 | 138 | 143 | PF00514 | 0.818 |
TRG_NLS_MonoExtC_3 | 138 | 143 | PF00514 | 0.818 |
TRG_NLS_MonoExtN_4 | 139 | 144 | PF00514 | 0.816 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P596 | Leptomonas seymouri | 42% | 96% |
A0A3Q8IL99 | Leishmania donovani | 88% | 100% |
A4HKN0 | Leishmania braziliensis | 74% | 100% |
A4I857 | Leishmania infantum | 88% | 100% |
D0AAC7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4Q536 | Leishmania major | 86% | 100% |