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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8ICW8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.633 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.512 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.488 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.468 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 378 | 388 | PF00069 | 0.726 |
DOC_MAPK_gen_1 | 82 | 91 | PF00069 | 0.615 |
DOC_MAPK_gen_1 | 99 | 110 | PF00069 | 0.483 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.586 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 11 | 15 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 160 | 168 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 171 | 178 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.720 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.717 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.456 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.512 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.666 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.674 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.673 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.743 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.594 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.541 |
LIG_LIR_Gen_1 | 29 | 37 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.601 |
LIG_PAM2_1 | 22 | 34 | PF00658 | 0.531 |
LIG_PDZ_Class_2 | 461 | 466 | PF00595 | 0.566 |
LIG_Pex14_2 | 335 | 339 | PF04695 | 0.720 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.443 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.623 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.582 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.725 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.458 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.593 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.679 |
MOD_CDK_SPxxK_3 | 164 | 171 | PF00069 | 0.754 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.724 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.818 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.505 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.750 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.680 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.751 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.809 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.440 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.614 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.744 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.673 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.480 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.677 |
MOD_GlcNHglycan | 278 | 282 | PF01048 | 0.693 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.637 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.735 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.733 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.608 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.543 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.797 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.659 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.708 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.614 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.624 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.495 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.646 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.728 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.616 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.597 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.474 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.724 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.695 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.577 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.675 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.639 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.555 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.472 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.456 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.515 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.662 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.552 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.588 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.749 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.724 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.576 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.558 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.683 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.754 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.649 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.698 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.704 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.671 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.605 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.580 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.746 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.715 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.672 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 397 | 407 | PF00179 | 0.720 |
MOD_SUMO_rev_2 | 430 | 438 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.623 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.531 |
TRG_NLS_MonoExtC_3 | 215 | 220 | PF00514 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE29 | Leptomonas seymouri | 67% | 98% |
A0A1X0P7K1 | Trypanosomatidae | 37% | 100% |
A0A3R7NTG2 | Trypanosoma rangeli | 36% | 100% |
A4HK15 | Leishmania braziliensis | 83% | 100% |
A4I7J9 | Leishmania infantum | 100% | 100% |
D0A0A1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B2F6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q5Q0 | Leishmania major | 96% | 100% |
V5BS76 | Trypanosoma cruzi | 33% | 100% |