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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8ISG1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.752 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.670 |
DEG_SCF_FBW7_1 | 109 | 116 | PF00400 | 0.670 |
DEG_SCF_FBW7_1 | 446 | 453 | PF00400 | 0.699 |
DOC_CKS1_1 | 110 | 115 | PF01111 | 0.725 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.717 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.635 |
DOC_CKS1_1 | 447 | 452 | PF01111 | 0.700 |
DOC_CYCLIN_yCln2_LP_2 | 378 | 384 | PF00134 | 0.568 |
DOC_MAPK_DCC_7 | 101 | 110 | PF00069 | 0.664 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 101 | 110 | PF00069 | 0.664 |
DOC_MAPK_MEF2A_6 | 14 | 21 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 299 | 306 | PF00069 | 0.493 |
DOC_MAPK_NFAT4_5 | 299 | 307 | PF00069 | 0.496 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.561 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.584 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.780 |
DOC_PP4_MxPP_1 | 422 | 425 | PF00568 | 0.746 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.653 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.854 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 251 | 255 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 299 | 303 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.621 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
LIG_BIR_III_4 | 10 | 14 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.746 |
LIG_CSL_BTD_1 | 317 | 320 | PF09270 | 0.713 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.626 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.654 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.494 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.708 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.621 |
LIG_IRF3_LxIS_1 | 191 | 197 | PF10401 | 0.675 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.672 |
LIG_LIR_Apic_2 | 253 | 257 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 336 | 342 | PF02991 | 0.594 |
LIG_LIR_Apic_2 | 477 | 481 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.754 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.674 |
LIG_LYPXL_S_1 | 230 | 234 | PF13949 | 0.580 |
LIG_LYPXL_yS_3 | 231 | 234 | PF13949 | 0.635 |
LIG_MAD2 | 101 | 109 | PF02301 | 0.546 |
LIG_NRBOX | 374 | 380 | PF00104 | 0.536 |
LIG_NRP_CendR_1 | 479 | 482 | PF00754 | 0.694 |
LIG_Pex14_1 | 96 | 100 | PF04695 | 0.609 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.654 |
LIG_PTB_Apo_2 | 94 | 101 | PF02174 | 0.608 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.756 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.521 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.674 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.746 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.651 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.651 |
LIG_SH2_PTP2 | 16 | 19 | PF00017 | 0.531 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.542 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 5 | 9 | PF00017 | 0.651 |
LIG_SH2_STAT3 | 187 | 190 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.542 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.685 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.757 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.634 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.662 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.728 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.708 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 275 | 282 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 275 | 282 | PF11976 | 0.670 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.586 |
MOD_CDK_SPK_2 | 113 | 118 | PF00069 | 0.718 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.793 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.592 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.674 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.814 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.575 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.852 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.674 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.674 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.679 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.665 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.674 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.615 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.723 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.683 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.562 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.513 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.647 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.620 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.714 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.596 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.594 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.609 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.669 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.651 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.629 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.665 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.770 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.643 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.695 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.617 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.710 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.699 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.664 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.629 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.617 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.720 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.507 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.683 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.667 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.621 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.658 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.685 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.747 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.573 |
MOD_PKA_1 | 55 | 61 | PF00069 | 0.759 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.757 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.487 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.507 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.619 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.661 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.628 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.730 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.628 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.620 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.556 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.694 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.662 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.680 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.846 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.579 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.617 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.783 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.767 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.578 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.671 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.661 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.733 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8K0 | Leptomonas seymouri | 43% | 100% |
A4HJ47 | Leishmania braziliensis | 68% | 100% |
A4I6G3 | Leishmania infantum | 100% | 100% |
E9B1M0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q6J4 | Leishmania major | 90% | 100% |