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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AMJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.567 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.615 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.596 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.590 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 60 | 69 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 36 | 39 | PF00134 | 0.534 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.660 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 73 | 77 | PF00244 | 0.774 |
LIG_Actin_WH2_2 | 124 | 140 | PF00022 | 0.739 |
LIG_BIR_III_2 | 219 | 223 | PF00653 | 0.476 |
LIG_BIR_III_2 | 413 | 417 | PF00653 | 0.770 |
LIG_BIR_III_4 | 329 | 333 | PF00653 | 0.616 |
LIG_BIR_III_4 | 96 | 100 | PF00653 | 0.692 |
LIG_Clathr_ClatBox_1 | 363 | 367 | PF01394 | 0.735 |
LIG_EVH1_2 | 38 | 42 | PF00568 | 0.700 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.745 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.550 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.505 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.826 |
LIG_GBD_Chelix_1 | 395 | 403 | PF00786 | 0.557 |
LIG_NRBOX | 127 | 133 | PF00104 | 0.772 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.570 |
LIG_PTAP_UEV_1 | 115 | 120 | PF05743 | 0.525 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.727 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.724 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.748 |
LIG_SUMO_SIM_par_1 | 299 | 305 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 360 | 368 | PF11976 | 0.727 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.701 |
LIG_WW_3 | 37 | 41 | PF00397 | 0.698 |
MOD_CDK_SPK_2 | 146 | 151 | PF00069 | 0.422 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.766 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.772 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.745 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.747 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.550 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.596 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.450 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.614 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.628 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.709 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.536 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.668 |
MOD_DYRK1A_RPxSP_1 | 429 | 433 | PF00069 | 0.495 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.710 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.768 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.650 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.709 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.679 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.597 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.701 |
MOD_GlcNHglycan | 407 | 411 | PF01048 | 0.579 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.735 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.786 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.813 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.739 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.797 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.624 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.677 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.569 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.581 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.666 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.730 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.709 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.687 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.638 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.627 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.688 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.683 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.510 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.598 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.750 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.721 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.728 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.603 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.614 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.682 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.715 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.595 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.613 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.595 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.713 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.696 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.801 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.634 |
MOD_Plk_2-3 | 473 | 479 | PF00069 | 0.727 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.772 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.745 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.621 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.695 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.730 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.711 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.753 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.710 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.720 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.665 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 341 | 347 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.599 |
TRG_DiLeu_LyEn_5 | 152 | 157 | PF01217 | 0.645 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 493 | 496 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.728 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 340 | 344 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK83 | Leptomonas seymouri | 43% | 100% |
A0A3S5H6A2 | Leishmania donovani | 89% | 100% |
A0A422NFT6 | Trypanosoma rangeli | 32% | 100% |
A4HC43 | Leishmania braziliensis | 73% | 99% |
E9AG89 | Leishmania infantum | 86% | 100% |
Q4QI40 | Leishmania major | 87% | 100% |
V5AUD8 | Trypanosoma cruzi | 32% | 100% |