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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4Q668
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 238 | 242 | PF00082 | 0.474 |
CLV_PCSK_FUR_1 | 418 | 422 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 108 | 114 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.606 |
CLV_Separin_Metazoa | 92 | 96 | PF03568 | 0.667 |
DEG_Kelch_Keap1_1 | 62 | 67 | PF01344 | 0.823 |
DEG_SCF_FBW7_2 | 85 | 92 | PF00400 | 0.681 |
DEG_SPOP_SBC_1 | 166 | 170 | PF00917 | 0.760 |
DEG_SPOP_SBC_1 | 374 | 378 | PF00917 | 0.660 |
DOC_AGCK_PIF_1 | 251 | 256 | PF00069 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 478 | 484 | PF00134 | 0.748 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.730 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.752 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.838 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.839 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.710 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.753 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.632 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.685 |
LIG_14-3-3_CanoR_1 | 129 | 134 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.826 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.739 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.736 |
LIG_Clathr_ClatBox_1 | 335 | 339 | PF01394 | 0.734 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.757 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.622 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.802 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.717 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.723 |
LIG_LIR_Apic_2 | 177 | 182 | PF02991 | 0.825 |
LIG_LIR_Gen_1 | 255 | 260 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.813 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.773 |
LIG_LYPXL_yS_3 | 332 | 335 | PF13949 | 0.813 |
LIG_MLH1_MIPbox_1 | 432 | 436 | PF16413 | 0.736 |
LIG_MYND_1 | 85 | 89 | PF01753 | 0.684 |
LIG_PCNA_yPIPBox_3 | 424 | 436 | PF02747 | 0.729 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.405 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.651 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.755 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.643 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.768 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.665 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.669 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.674 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.677 |
LIG_WW_3 | 83 | 87 | PF00397 | 0.624 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.719 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.727 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.704 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.683 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.564 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.675 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.729 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.705 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.675 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.720 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.814 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.798 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.623 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.746 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.576 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.653 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.630 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.717 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.439 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.721 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.703 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.729 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.603 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.718 |
MOD_GlcNHglycan | 281 | 285 | PF01048 | 0.643 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.539 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.697 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.692 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.687 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.711 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.681 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.647 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.759 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.654 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.717 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.729 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.648 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.700 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.630 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.710 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.671 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.692 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.579 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.718 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.618 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.770 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.754 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.690 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.604 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.575 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.707 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.647 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.717 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.553 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.803 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.679 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.650 |
MOD_OFUCOSY | 297 | 302 | PF10250 | 0.577 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.591 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.578 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.672 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.825 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.692 |
MOD_PK_1 | 129 | 135 | PF00069 | 0.498 |
MOD_PK_1 | 309 | 315 | PF00069 | 0.732 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.699 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.591 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.703 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.587 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.814 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.575 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.589 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.626 |
MOD_PKB_1 | 290 | 298 | PF00069 | 0.754 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.650 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.677 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.824 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.557 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.559 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.810 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.602 |
TRG_DiLeu_BaEn_2 | 329 | 335 | PF01217 | 0.647 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.682 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 238 | 241 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.615 |
TRG_NLS_MonoCore_2 | 102 | 107 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 101 | 107 | PF00514 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.701 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGX0 | Leptomonas seymouri | 42% | 99% |
A0A3Q8IGF6 | Leishmania donovani | 89% | 100% |
A4HJH6 | Leishmania braziliensis | 59% | 100% |
A4HJX3 | Leishmania braziliensis | 59% | 100% |
A4I6W9 | Leishmania infantum | 89% | 100% |
E9B1Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |